{"gene":"PF3D7_1351700","run_date":"2026-09-08T16:26:55","timeline":{"discoveries":[{"year":2025,"finding":"IMC1f (PF3D7_1351700) localizes to the basal complex in P. falciparum asexual blood stages, but is dispensable for parasite replication — direct knockout of PfIMC1f caused no detectable growth defect. Furthermore, simultaneous knockout of both PfIMC1f and PfIMC1e (a paralog that also localizes to the basal complex) likewise caused no difference in parasite replication, demonstrating that these two proteins are not redundant with each other for asexual growth.","method":"Direct gene knockout (PfIMC1f KO), inducible DiCre/loxP conditional knockout (PfIMC1e iKO), flow cytometry growth assay, immunofluorescence assay (IFA) with endogenous smHA tag","journal":"Cellular microbiology","confidence":"Medium","confidence_rationale":"Tier 2 / Moderate — clean KO with defined growth phenotype and IFA localization, single lab, two orthogonal methods (genetic KO + IFA)","pmids":["41019501"],"is_preprint":false,"attribution":[{"species":"Plasmodium falciparum","strain":""}]},{"year":2025,"finding":"PfIMC1e requires PfIMC1f for its sequential recruitment to the basal complex — in cells lacking PfIMC1f, PfIMC1e fails to localize properly to the basal complex, establishing a hierarchical dependency between these two alveolins for basal complex targeting.","method":"IFA with endogenous smV5-tagged PfIMC1e in the PfIMC1f KO background; inducible DiCre/loxP conditional KO of PfIMC1e","journal":"Cellular microbiology","confidence":"Medium","confidence_rationale":"Tier 2 / Moderate — direct localization experiment with loss-of-function showing specific recruitment dependency, single lab, two orthogonal methods (genetic KO + IFA)","pmids":["41019501"],"is_preprint":false,"attribution":[{"species":"Plasmodium falciparum","strain":""}]},{"year":2026,"finding":"IMC1f localizes to the basal complex only at the late 'separation' step of basal complex development during schizogony — it is not detectable at the earlier C-shaped initiation or enlargement steps, and forms a complete ring structure at the basal complex by the beginning of segmentation.","method":"Ultrastructure expansion microscopy (U-ExM) with smV5-tagged IMC1f in the background of BTP2 inducible knockout parasites; DNA-PAINT nanoscale imaging","journal":"Science advances","confidence":"Medium","confidence_rationale":"Tier 2 / Moderate — direct localization experiment with high-resolution imaging (U-ExM), single lab, two orthogonal imaging methods","pmids":["41706859"],"is_preprint":false,"attribution":[{"species":"Plasmodium falciparum","strain":""}]},{"year":2014,"finding":"IMC1f contains both type 1 and type 2 alveolin repeat domains arranged tandemly within a single uninterrupted block of conserved sequence, suggesting that type 1 and type 2 alveolin domains are structurally related despite low primary sequence similarity.","method":"Computational domain analysis and structural comparison of alveolin repeat sequences across Plasmodium family members","journal":"Parasitology research","confidence":"Low","confidence_rationale":"Tier 4 / Weak — computational/bioinformatic analysis only, no functional experimental validation specific to IMC1f","pmids":["25475193"],"is_preprint":false,"attribution":[{"species":"Plasmodium falciparum","strain":""}]}],"current_model":"IMC1f (PF3D7_1351700) is a P. falciparum alveolin that localizes to the basal complex late in schizogony (only at the separation step, forming a complete ring at the onset of segmentation); it is individually dispensable for asexual blood-stage replication, is not redundant with its paralog PfIMC1e, and acts upstream of PfIMC1e by being required for PfIMC1e's sequential recruitment to the basal complex."},"narrative":{"mechanistic_narrative":"IMC1f (PF3D7_1351700) is a Plasmodium falciparum alveolin that localizes to the basal complex during asexual blood-stage schizogony [PMID:41019501]. Its recruitment is temporally restricted: IMC1f is undetectable at the early C-shaped initiation and enlargement steps of basal complex development, appearing only at the late 'separation' step and forming a complete ring at the onset of segmentation [PMID:41706859]. IMC1f acts upstream of its paralog PfIMC1e, being required for the sequential recruitment of PfIMC1e to the basal complex, establishing a hierarchical targeting dependency between these two alveolins [PMID:41019501]. Despite this role, IMC1f is individually dispensable for asexual replication, and combined loss of IMC1f and PfIMC1e produces no growth defect, indicating the two paralogs are not functionally redundant for asexual growth [PMID:41019501]. Beyond its basal-complex localization, its recruitment hierarchy, and its predicted alveolin repeat architecture, no further mechanistic detail — including binding partners or the molecular basis of its recruitment — has been characterized for IMC1f in the available corpus.","teleology":[{"year":2014,"claim":"Before functional data existed, the question was what structural class IMC1f belongs to; sequence analysis placed it in the alveolin family, framing it as a cytoskeletal/pellicle-associated protein.","evidence":"Computational domain and structural comparison of alveolin repeat sequences across Plasmodium family members","pmids":["25475193"],"confidence":"Low","gaps":["Computational prediction only, with no functional experimental validation specific to IMC1f","No experimental evidence that the tandem type 1/type 2 alveolin domains form the predicted structure","No cellular localization or interaction data at this stage"],"attribution":[{"species":"Plasmodium falciparum","strain":""}]},{"year":2025,"claim":"It was unknown where IMC1f acts and whether it is essential; knockout established it localizes to the basal complex yet is individually dispensable and non-redundant with its paralog PfIMC1e for asexual replication.","evidence":"Direct gene knockout, DiCre/loxP conditional knockout, flow cytometry growth assay, and IFA with endogenous smHA tag in P. falciparum asexual blood stages","pmids":["41019501"],"confidence":"Medium","gaps":["No growth phenotype leaves the specific asexual function of IMC1f undefined","Whether IMC1f contributes to sexual stages or transmission was not tested","No binding partners or biochemical activity identified"],"attribution":[{"species":"Plasmodium falciparum","strain":""}]},{"year":2025,"claim":"The relationship between the two basal-complex alveolins was unknown; loss-of-function showed IMC1f is required for PfIMC1e recruitment, establishing a hierarchical assembly order.","evidence":"IFA of endogenous smV5-tagged PfIMC1e in the PfIMC1f knockout background, plus DiCre/loxP conditional knockout of PfIMC1e in P. falciparum","pmids":["41019501"],"confidence":"Medium","gaps":["The molecular mechanism by which IMC1f enables PfIMC1e recruitment (direct binding vs. indirect scaffolding) is unresolved","Whether IMC1f recruits additional basal-complex components beyond PfIMC1e is unknown","No reciprocal test of whether PfIMC1e influences IMC1f localization reported here"],"attribution":[{"species":"Plasmodium falciparum","strain":""}]},{"year":2026,"claim":"The timing of IMC1f arrival at the basal complex was unknown; high-resolution imaging placed its recruitment specifically at the late separation step, refining it as a marker of the mature, segmenting basal complex.","evidence":"Ultrastructure expansion microscopy (U-ExM) and DNA-PAINT nanoscale imaging of smV5-tagged IMC1f in a BTP2 inducible knockout background in P. falciparum","pmids":["41706859"],"confidence":"Medium","gaps":["The trigger controlling IMC1f's late, separation-stage-specific recruitment is unknown","The functional consequence of ring formation at segmentation onset is not defined","Relationship between recruitment timing and the IMC1f→PfIMC1e hierarchy not directly integrated"],"attribution":[{"species":"Plasmodium falciparum","strain":""}]},{"year":null,"claim":"The direct molecular function of IMC1f — its binding partners, the structural basis of its basal-complex targeting, and its role (if any) in stages beyond asexual replication — remains unresolved.","evidence":"","pmids":[],"confidence":"Medium","gaps":["No direct interaction partners of IMC1f identified","No structural or biochemical characterization of the alveolin domains in vitro","Its function outside asexual blood stages, where it is dispensable, is untested"],"attribution":[{"species":"Plasmodium falciparum","strain":""}]}],"mechanism_profile":{"molecular_activity":[],"localization":[],"pathway":[],"complexes":["Basal complex (P. falciparum, asexual schizogony)"],"partners":["PFIMC1E (PARALOGOUS ALVEOLIN; IMC1F REQUIRED FOR ITS RECRUITMENT TO THE BASAL COMPLEX)"],"other_free_text":["Alveolin containing tandem type 1 and type 2 alveolin repeat domains within a single conserved block [#3].","Recruited to the basal complex only at the late 'separation' step, forming a complete ring at the onset of segmentation [#2].","Individually dispensable for asexual replication and non-redundant with PfIMC1e [#0].","Acts upstream of PfIMC1e in a hierarchical basal-complex targeting dependency [#1]."]}},"prefetch_data":{},"corpus_meta":[{"pmid":"37712738","id":"PMC_37712738","title":"Essential function of alveolin PfIMC1g in the Plasmodium falciparum asexual blood stage.","date":"2023","source":"mBio","url":"https://pubmed.ncbi.nlm.nih.gov/37712738","citation_count":25,"is_preprint":false,"source_species":["Pf"],"role":"primary","match_terms":["curated_ref"],"competing_organism_flag":false,"competing_organism_match":"","competing_organism_only":false},{"pmid":"41706859","id":"","title":"Transmembrane proteins mediate basal complex assembly and individual daughter cell formation in malaria parasites.","date":"2026","source":"Science advances","url":"https://pubmed.ncbi.nlm.nih.gov/41706859","citation_count":0,"is_preprint":false,"source_species":["Pf"],"role":"primary","match_terms":["IMC1f"],"competing_organism_flag":false,"competing_organism_match":"","competing_organism_only":false},{"pmid":"41019501","id":"","title":"Malaria Cytoskeletal Proteins Require Alveolin-Alveolin Interactions for Differential Localization: Recruitment and Organization of Alveolin Proteins.","date":"2025","source":"Cellular microbiology","url":"https://pubmed.ncbi.nlm.nih.gov/41019501","citation_count":0,"is_preprint":false,"source_species":["Pf"],"role":"primary","match_terms":["IMC1f"],"competing_organism_flag":false,"competing_organism_match":"","competing_organism_only":false},{"pmid":"42294623","id":"","title":"Plasmodium falciparum leucine-rich repeat 5 disruption alters the transcription progression during asexual and sexual stage development.","date":"2026","source":"mSphere","url":"https://pubmed.ncbi.nlm.nih.gov/42294623","citation_count":0,"is_preprint":false,"source_species":["Pf"],"role":"primary","match_terms":["IMC1f"],"competing_organism_flag":false,"competing_organism_match":"","competing_organism_only":false},{"pmid":"36750737","id":"","title":"Population genetic analysis of Plasmodium knowlesi reveals differential selection and exchange events between Borneo and Peninsular sub-populations.","date":"2023","source":"Scientific reports","url":"https://pubmed.ncbi.nlm.nih.gov/36750737","citation_count":0,"is_preprint":false,"source_species":["Pf"],"role":"primary","match_terms":["IMC1f"],"competing_organism_flag":false,"competing_organism_match":"","competing_organism_only":false},{"pmid":"35775739","id":"","title":"Inner membrane complex proteomics reveals a palmitoylation regulation critical for intraerythrocytic development of malaria parasite.","date":"2022","source":"eLife","url":"https://pubmed.ncbi.nlm.nih.gov/35775739","citation_count":0,"is_preprint":false,"source_species":["Pf"],"role":"primary","match_terms":["IMC1f"],"competing_organism_flag":false,"competing_organism_match":"","competing_organism_only":false},{"pmid":"35938722","id":"","title":"The Plasmodium falciparum Nuclear Protein Phosphatase NIF4 Is Required for Efficient Merozoite Invasion and Regulates Artemisinin Sensitivity.","date":"2022","source":"mBio","url":"https://pubmed.ncbi.nlm.nih.gov/35938722","citation_count":0,"is_preprint":false,"source_species":["Pf"],"role":"primary","match_terms":["IMC1f"],"competing_organism_flag":false,"competing_organism_match":"","competing_organism_only":false},{"pmid":"33489940","id":"","title":"The Dynamic Roles of the Inner Membrane Complex in the Multiple Stages of the Malaria Parasite.","date":"2021","source":"Frontiers in cellular and infection microbiology","url":"https://pubmed.ncbi.nlm.nih.gov/33489940","citation_count":0,"is_preprint":false,"source_species":["Pf"],"role":"primary","match_terms":["IMC1f"],"competing_organism_flag":false,"competing_organism_match":"","competing_organism_only":false},{"pmid":"29580379","id":"","title":"Single-cell RNA-seq reveals hidden transcriptional variation in malaria parasites.","date":"2018","source":"eLife","url":"https://pubmed.ncbi.nlm.nih.gov/29580379","citation_count":0,"is_preprint":false,"source_species":["Pf"],"role":"primary","match_terms":["IMC1f"],"competing_organism_flag":false,"competing_organism_match":"","competing_organism_only":false},{"pmid":"25475193","id":"","title":"Plasmodium alveolins possess distinct but structurally and functionally related multi-repeat domains.","date":"2014","source":"Parasitology research","url":"https://pubmed.ncbi.nlm.nih.gov/25475193","citation_count":0,"is_preprint":false,"source_species":["Pf"],"role":"primary","match_terms":["IMC1f"],"competing_organism_flag":false,"competing_organism_match":"","competing_organism_only":false}],"cost":{"stage1":{"model":"claude-sonnet-4-6","input_tokens":13721,"output_tokens":1195,"usd":0.029544,"stage1_stop_reason":"end_turn"},"stage2":{"model":"claude-opus-4-8","input_tokens":6047,"output_tokens":2390,"usd":0.044992,"stage2_stop_reason":"end_turn"},"total_usd":0.074536,"stage1_batch_id":"msgbatch_01NE1MTa8x1hW7Lo4tAaNzY1","stage2_batch_id":"msgbatch_0141vaQdeFvbo2q39AinvXM9","note":"batch pricing = 50% of standard"},"stage1_raw":"```json\n{\n  \"discoveries\": [\n    {\n      \"year\": 2025,\n      \"finding\": \"IMC1f (PF3D7_1351700) localizes to the basal complex in P. falciparum asexual blood stages, but is dispensable for parasite replication — direct knockout of PfIMC1f caused no detectable growth defect. Furthermore, simultaneous knockout of both PfIMC1f and PfIMC1e (a paralog that also localizes to the basal complex) likewise caused no difference in parasite replication, demonstrating that these two proteins are not redundant with each other for asexual growth.\",\n      \"method\": \"Direct gene knockout (PfIMC1f KO), inducible DiCre/loxP conditional knockout (PfIMC1e iKO), flow cytometry growth assay, immunofluorescence assay (IFA) with endogenous smHA tag\",\n      \"journal\": \"Cellular microbiology\",\n      \"confidence\": \"Medium\",\n      \"confidence_rationale\": \"Tier 2 / Moderate — clean KO with defined growth phenotype and IFA localization, single lab, two orthogonal methods (genetic KO + IFA)\",\n      \"pmids\": [\"41019501\"],\n      \"is_preprint\": false,\n      \"attribution\": [{\"species\": \"Plasmodium falciparum\", \"strain\": \"\"}]\n    },\n    {\n      \"year\": 2025,\n      \"finding\": \"PfIMC1e requires PfIMC1f for its sequential recruitment to the basal complex — in cells lacking PfIMC1f, PfIMC1e fails to localize properly to the basal complex, establishing a hierarchical dependency between these two alveolins for basal complex targeting.\",\n      \"method\": \"IFA with endogenous smV5-tagged PfIMC1e in the PfIMC1f KO background; inducible DiCre/loxP conditional KO of PfIMC1e\",\n      \"journal\": \"Cellular microbiology\",\n      \"confidence\": \"Medium\",\n      \"confidence_rationale\": \"Tier 2 / Moderate — direct localization experiment with loss-of-function showing specific recruitment dependency, single lab, two orthogonal methods (genetic KO + IFA)\",\n      \"pmids\": [\"41019501\"],\n      \"is_preprint\": false,\n      \"attribution\": [{\"species\": \"Plasmodium falciparum\", \"strain\": \"\"}]\n    },\n    {\n      \"year\": 2026,\n      \"finding\": \"IMC1f localizes to the basal complex only at the late 'separation' step of basal complex development during schizogony — it is not detectable at the earlier C-shaped initiation or enlargement steps, and forms a complete ring structure at the basal complex by the beginning of segmentation.\",\n      \"method\": \"Ultrastructure expansion microscopy (U-ExM) with smV5-tagged IMC1f in the background of BTP2 inducible knockout parasites; DNA-PAINT nanoscale imaging\",\n      \"journal\": \"Science advances\",\n      \"confidence\": \"Medium\",\n      \"confidence_rationale\": \"Tier 2 / Moderate — direct localization experiment with high-resolution imaging (U-ExM), single lab, two orthogonal imaging methods\",\n      \"pmids\": [\"41706859\"],\n      \"is_preprint\": false,\n      \"attribution\": [{\"species\": \"Plasmodium falciparum\", \"strain\": \"\"}]\n    },\n    {\n      \"year\": 2014,\n      \"finding\": \"IMC1f contains both type 1 and type 2 alveolin repeat domains arranged tandemly within a single uninterrupted block of conserved sequence, suggesting that type 1 and type 2 alveolin domains are structurally related despite low primary sequence similarity.\",\n      \"method\": \"Computational domain analysis and structural comparison of alveolin repeat sequences across Plasmodium family members\",\n      \"journal\": \"Parasitology research\",\n      \"confidence\": \"Low\",\n      \"confidence_rationale\": \"Tier 4 / Weak — computational/bioinformatic analysis only, no functional experimental validation specific to IMC1f\",\n      \"pmids\": [\"25475193\"],\n      \"is_preprint\": false,\n      \"attribution\": [{\"species\": \"Plasmodium falciparum\", \"strain\": \"\"}]\n    }\n  ],\n  \"current_model\": \"IMC1f (PF3D7_1351700) is a P. falciparum alveolin that localizes to the basal complex late in schizogony (only at the separation step, forming a complete ring at the onset of segmentation); it is individually dispensable for asexual blood-stage replication, is not redundant with its paralog PfIMC1e, and acts upstream of PfIMC1e by being required for PfIMC1e's sequential recruitment to the basal complex.\"\n}\n```","stage2_raw":"{\n  \"mechanistic_narrative\": \"IMC1f (PF3D7_1351700) is a Plasmodium falciparum alveolin that localizes to the basal complex during asexual blood-stage schizogony [#0]. Its recruitment is temporally restricted: IMC1f is undetectable at the early C-shaped initiation and enlargement steps of basal complex development, appearing only at the late 'separation' step and forming a complete ring at the onset of segmentation [#2]. IMC1f acts upstream of its paralog PfIMC1e, being required for the sequential recruitment of PfIMC1e to the basal complex, establishing a hierarchical targeting dependency between these two alveolins [#1]. Despite this role, IMC1f is individually dispensable for asexual replication, and combined loss of IMC1f and PfIMC1e produces no growth defect, indicating the two paralogs are not functionally redundant for asexual growth [#0]. Beyond its basal-complex localization, its recruitment hierarchy, and its predicted alveolin repeat architecture, no further mechanistic detail — including binding partners or the molecular basis of its recruitment — has been characterized for IMC1f in the available corpus.\",\n  \"teleology\": [\n    {\n      \"year\": 2014,\n      \"claim\": \"Before functional data existed, the question was what structural class IMC1f belongs to; sequence analysis placed it in the alveolin family, framing it as a cytoskeletal/pellicle-associated protein.\",\n      \"evidence\": \"Computational domain and structural comparison of alveolin repeat sequences across Plasmodium family members\",\n      \"pmids\": [\"25475193\"],\n      \"confidence\": \"Low\",\n      \"gaps\": [\n        \"Computational prediction only, with no functional experimental validation specific to IMC1f\",\n        \"No experimental evidence that the tandem type 1/type 2 alveolin domains form the predicted structure\",\n        \"No cellular localization or interaction data at this stage\"\n      ],\n      \"attribution\": [\n        {\"species\": \"Plasmodium falciparum\", \"strain\": \"\"}\n      ]\n    },\n    {\n      \"year\": 2025,\n      \"claim\": \"It was unknown where IMC1f acts and whether it is essential; knockout established it localizes to the basal complex yet is individually dispensable and non-redundant with its paralog PfIMC1e for asexual replication.\",\n      \"evidence\": \"Direct gene knockout, DiCre/loxP conditional knockout, flow cytometry growth assay, and IFA with endogenous smHA tag in P. falciparum asexual blood stages\",\n      \"pmids\": [\"41019501\"],\n      \"confidence\": \"Medium\",\n      \"gaps\": [\n        \"No growth phenotype leaves the specific asexual function of IMC1f undefined\",\n        \"Whether IMC1f contributes to sexual stages or transmission was not tested\",\n        \"No binding partners or biochemical activity identified\"\n      ],\n      \"attribution\": [\n        {\"species\": \"Plasmodium falciparum\", \"strain\": \"\"}\n      ]\n    },\n    {\n      \"year\": 2025,\n      \"claim\": \"The relationship between the two basal-complex alveolins was unknown; loss-of-function showed IMC1f is required for PfIMC1e recruitment, establishing a hierarchical assembly order.\",\n      \"evidence\": \"IFA of endogenous smV5-tagged PfIMC1e in the PfIMC1f knockout background, plus DiCre/loxP conditional knockout of PfIMC1e in P. falciparum\",\n      \"pmids\": [\"41019501\"],\n      \"confidence\": \"Medium\",\n      \"gaps\": [\n        \"The molecular mechanism by which IMC1f enables PfIMC1e recruitment (direct binding vs. indirect scaffolding) is unresolved\",\n        \"Whether IMC1f recruits additional basal-complex components beyond PfIMC1e is unknown\",\n        \"No reciprocal test of whether PfIMC1e influences IMC1f localization reported here\"\n      ],\n      \"attribution\": [\n        {\"species\": \"Plasmodium falciparum\", \"strain\": \"\"}\n      ]\n    },\n    {\n      \"year\": 2026,\n      \"claim\": \"The timing of IMC1f arrival at the basal complex was unknown; high-resolution imaging placed its recruitment specifically at the late separation step, refining it as a marker of the mature, segmenting basal complex.\",\n      \"evidence\": \"Ultrastructure expansion microscopy (U-ExM) and DNA-PAINT nanoscale imaging of smV5-tagged IMC1f in a BTP2 inducible knockout background in P. falciparum\",\n      \"pmids\": [\"41706859\"],\n      \"confidence\": \"Medium\",\n      \"gaps\": [\n        \"The trigger controlling IMC1f's late, separation-stage-specific recruitment is unknown\",\n        \"The functional consequence of ring formation at segmentation onset is not defined\",\n        \"Relationship between recruitment timing and the IMC1f→PfIMC1e hierarchy not directly integrated\"\n      ],\n      \"attribution\": [\n        {\"species\": \"Plasmodium falciparum\", \"strain\": \"\"}\n      ]\n    },\n    {\n      \"year\": null,\n      \"claim\": \"The direct molecular function of IMC1f — its binding partners, the structural basis of its basal-complex targeting, and its role (if any) in stages beyond asexual replication — remains unresolved.\",\n      \"evidence\": \"\",\n      \"pmids\": [],\n      \"confidence\": \"Medium\",\n      \"gaps\": [\n        \"No direct interaction partners of IMC1f identified\",\n        \"No structural or biochemical characterization of the alveolin domains in vitro\",\n        \"Its function outside asexual blood stages, where it is dispensable, is untested\"\n      ],\n      \"attribution\": [\n        {\"species\": \"Plasmodium falciparum\", \"strain\": \"\"}\n      ]\n    }\n  ],\n  \"mechanism_profile\": {\n    \"molecular_activity\": [\n      {\"term_id\": \"GO:0005200\", \"supporting_discovery_ids\": [3]}\n    ],\n    \"localization\": [\n      {\"term_id\": \"GO:0020039\", \"supporting_discovery_ids\": [0, 2]}\n    ],\n    \"pathway\": [\n      {\"term_id\": \"GO:0007049\", \"supporting_discovery_ids\": [0, 2]}\n    ],\n    \"complexes\": [\n      \"Basal complex (P. falciparum, asexual schizogony)\"\n    ],\n    \"partners\": [\n      \"PfIMC1e (paralogous alveolin; IMC1f required for its recruitment to the basal complex)\"\n    ],\n    \"other_free_text\": [\n      \"Alveolin containing tandem type 1 and type 2 alveolin repeat domains within a single conserved block [#3].\",\n      \"Recruited to the basal complex only at the late 'separation' step, forming a complete ring at the onset of segmentation [#2].\",\n      \"Individually dispensable for asexual replication and non-redundant with PfIMC1e [#0].\",\n      \"Acts upstream of PfIMC1e in a hierarchical basal-complex targeting dependency [#1].\"\n    ]\n  }\n}","audit_flag":null,"strains":[{"strain":"Pf3D7","gene_id":"PF3D7_1351700","name":null,"product":"inner membrane complex protein 1f","uniprot_acc":null,"chromosome":null,"start_pos":null},{"strain":"PbANKA","gene_id":"PBANKA_1364400","name":null,"product":"inner membrane complex protein 1f, putative","uniprot_acc":null,"chromosome":null,"start_pos":null},{"strain":"PkH","gene_id":"PKNH_1249300","name":null,"product":"inner membrane complex protein 1f, putative","uniprot_acc":null,"chromosome":null,"start_pos":null}],"gene_symbol":"IMC1f","evaluation":null}