Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005739 | mitochondrion | 5 | 2 |
GO:0009331 | glycerol-3-phosphate dehydrogenase complex | 4 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:1902494 | catalytic complex | 2 | 12 |
GO:1990204 | oxidoreductase complex | 3 | 12 |
GO:0016020 | membrane | 2 | 2 |
Related structures:
AlphaFold database: Q4Q8P6
Term | Name | Level | Count |
---|---|---|---|
GO:0006072 | glycerol-3-phosphate metabolic process | 5 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0019637 | organophosphate metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0052646 | alditol phosphate metabolic process | 4 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004368 | glycerol-3-phosphate dehydrogenase (quinone) activity | 5 | 12 |
GO:0005488 | binding | 1 | 2 |
GO:0016491 | oxidoreductase activity | 2 | 12 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 12 |
GO:0016901 | oxidoreductase activity, acting on the CH-OH group of donors, quinone or similar compound as acceptor | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 2 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 2 |
GO:0052590 | sn-glycerol-3-phosphate:ubiquinone oxidoreductase activity | 6 | 12 |
GO:0052591 | sn-glycerol-3-phosphate:ubiquinone-8 oxidoreductase activity | 7 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901265 | nucleoside phosphate binding | 3 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 210 | 214 | PF00656 | 0.474 |
CLV_C14_Caspase3-7 | 82 | 86 | PF00656 | 0.469 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.317 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.361 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 446 | 448 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.252 |
CLV_PCSK_KEX2_1 | 557 | 559 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 590 | 592 | PF00082 | 0.397 |
CLV_PCSK_PC1ET2_1 | 590 | 592 | PF00082 | 0.397 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 302 | 306 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 560 | 564 | PF00082 | 0.277 |
CLV_Separin_Metazoa | 267 | 271 | PF03568 | 0.557 |
DOC_CDC14_PxL_1 | 146 | 154 | PF14671 | 0.463 |
DOC_CDC14_PxL_1 | 201 | 209 | PF14671 | 0.538 |
DOC_CKS1_1 | 369 | 374 | PF01111 | 0.418 |
DOC_MAPK_FxFP_2 | 194 | 197 | PF00069 | 0.538 |
DOC_MAPK_gen_1 | 330 | 337 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 557 | 563 | PF00069 | 0.463 |
DOC_PP1_RVXF_1 | 341 | 347 | PF00149 | 0.452 |
DOC_PP1_RVXF_1 | 558 | 564 | PF00149 | 0.440 |
DOC_PP2B_LxvP_1 | 405 | 408 | PF13499 | 0.513 |
DOC_PP2B_LxvP_1 | 493 | 496 | PF13499 | 0.557 |
DOC_PP4_FxxP_1 | 194 | 197 | PF00568 | 0.463 |
DOC_PP4_FxxP_1 | 346 | 349 | PF00568 | 0.513 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.514 |
DOC_USP7_UBL2_3 | 202 | 206 | PF12436 | 0.513 |
DOC_USP7_UBL2_3 | 459 | 463 | PF12436 | 0.592 |
DOC_USP7_UBL2_3 | 465 | 469 | PF12436 | 0.590 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.538 |
LIG_14-3-3_CanoR_1 | 232 | 238 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 575 | 583 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 89 | 94 | PF00244 | 0.455 |
LIG_Actin_WH2_2 | 117 | 135 | PF00022 | 0.493 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.425 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.462 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.499 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.482 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.470 |
LIG_FHA_1 | 416 | 422 | PF00498 | 0.477 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.438 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.562 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.466 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.468 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.470 |
LIG_FHA_2 | 303 | 309 | PF00498 | 0.390 |
LIG_LIR_Apic_2 | 192 | 197 | PF02991 | 0.477 |
LIG_LIR_Apic_2 | 24 | 28 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 248 | 259 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 188 | 194 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 397 | 402 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 509 | 514 | PF02991 | 0.452 |
LIG_LYPXL_yS_3 | 204 | 207 | PF13949 | 0.538 |
LIG_MYND_1 | 157 | 161 | PF01753 | 0.538 |
LIG_NRP_CendR_1 | 606 | 608 | PF00754 | 0.278 |
LIG_Pex14_1 | 503 | 507 | PF04695 | 0.452 |
LIG_Pex14_2 | 346 | 350 | PF04695 | 0.452 |
LIG_SH2_CRK | 25 | 29 | PF00017 | 0.554 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.538 |
LIG_SH2_CRK | 599 | 603 | PF00017 | 0.600 |
LIG_SH2_GRB2like | 25 | 28 | PF00017 | 0.554 |
LIG_SH2_NCK_1 | 25 | 29 | PF00017 | 0.586 |
LIG_SH2_NCK_1 | 45 | 49 | PF00017 | 0.381 |
LIG_SH2_SRC | 8 | 11 | PF00017 | 0.374 |
LIG_SH2_STAP1 | 178 | 182 | PF00017 | 0.448 |
LIG_SH2_STAP1 | 235 | 239 | PF00017 | 0.557 |
LIG_SH2_STAP1 | 285 | 289 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 599 | 603 | PF00017 | 0.619 |
LIG_SH2_STAT3 | 224 | 227 | PF00017 | 0.435 |
LIG_SH2_STAT3 | 541 | 544 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.452 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.509 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.509 |
LIG_SUMO_SIM_anti_2 | 473 | 480 | PF11976 | 0.418 |
LIG_SUMO_SIM_anti_2 | 69 | 74 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 280 | 286 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 424 | 430 | PF11976 | 0.457 |
LIG_TYR_ITIM | 249 | 254 | PF00017 | 0.493 |
LIG_TYR_ITIM | 43 | 48 | PF00017 | 0.626 |
LIG_UBA3_1 | 435 | 442 | PF00899 | 0.515 |
LIG_UBA3_1 | 524 | 530 | PF00899 | 0.523 |
LIG_WRC_WIRS_1 | 602 | 607 | PF05994 | 0.514 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.460 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.513 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.531 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.524 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.523 |
MOD_CK2_1 | 302 | 308 | PF00069 | 0.390 |
MOD_GlcNHglycan | 190 | 194 | PF01048 | 0.291 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.356 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.273 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.277 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.415 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.274 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.410 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.462 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.444 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.501 |
MOD_GSK3_1 | 597 | 604 | PF00069 | 0.600 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.449 |
MOD_N-GLC_1 | 436 | 441 | PF02516 | 0.329 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.463 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.513 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.477 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.453 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.483 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.474 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.514 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.538 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.512 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.536 |
MOD_NEK2_2 | 601 | 606 | PF00069 | 0.519 |
MOD_PIKK_1 | 28 | 34 | PF00454 | 0.535 |
MOD_PIKK_1 | 415 | 421 | PF00454 | 0.477 |
MOD_PK_1 | 44 | 50 | PF00069 | 0.455 |
MOD_PK_1 | 89 | 95 | PF00069 | 0.477 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.448 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.474 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.555 |
MOD_PKA_2 | 556 | 562 | PF00069 | 0.452 |
MOD_PKA_2 | 574 | 580 | PF00069 | 0.550 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.493 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.548 |
MOD_Plk_4 | 155 | 161 | PF00069 | 0.452 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.503 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.418 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.538 |
MOD_SUMO_for_1 | 43 | 46 | PF00179 | 0.611 |
MOD_SUMO_rev_2 | 424 | 433 | PF00179 | 0.529 |
TRG_DiLeu_BaEn_2 | 189 | 195 | PF01217 | 0.557 |
TRG_ENDOCYTIC_2 | 163 | 166 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.434 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.477 |
TRG_ENDOCYTIC_2 | 446 | 449 | PF00928 | 0.494 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.626 |
TRG_ENDOCYTIC_2 | 511 | 514 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 599 | 602 | PF00928 | 0.596 |
TRG_ER_diArg_1 | 557 | 560 | PF00400 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 270 | 274 | PF00026 | 0.301 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDC6 | Leptomonas seymouri | 68% | 100% |
A0A0S4IY53 | Bodo saltans | 42% | 95% |
A0A1X0NVE3 | Trypanosomatidae | 54% | 99% |
A0A3Q8IDM8 | Leishmania donovani | 95% | 100% |
A0A422N0G9 | Trypanosoma rangeli | 56% | 100% |
A4HG65 | Leishmania braziliensis | 86% | 100% |
A4I397 | Leishmania infantum | 95% | 100% |
A6QLU1 | Bos taurus | 36% | 84% |
A7DZP8 | Mesocricetus auratus | 38% | 84% |
D0A7S4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
D4GQU6 | Haloferax volcanii (strain ATCC 29605 / DSM 3757 / JCM 8879 / NBRC 14742 / NCIMB 2012 / VKM B-1768 / DS2) | 24% | 100% |
E9AZI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
O14400 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 94% |
O83004 | Pseudomonas tolaasii | 25% | 100% |
O86963 | Enterococcus casseliflavus | 28% | 100% |
P0A9C0 | Escherichia coli (strain K12) | 24% | 100% |
P0A9C1 | Escherichia coli O157:H7 | 24% | 100% |
P0A9C2 | Shigella flexneri | 24% | 100% |
P0DB20 | Streptococcus pyogenes serotype M3 (strain ATCC BAA-595 / MGAS315) | 27% | 99% |
P0DB21 | Streptococcus pyogenes serotype M3 (strain SSI-1) | 27% | 99% |
P13035 | Escherichia coli (strain K12) | 26% | 100% |
P18158 | Bacillus subtilis (strain 168) | 31% | 100% |
P32191 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 33% | 94% |
P35571 | Rattus norvegicus | 36% | 84% |
P35596 | Streptococcus pneumoniae serotype 4 (strain ATCC BAA-334 / TIGR4) | 27% | 100% |
P43304 | Homo sapiens | 36% | 84% |
P43799 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 24% | 100% |
P52111 | Pseudomonas aeruginosa (strain ATCC 15692 / DSM 22644 / CIP 104116 / JCM 14847 / LMG 12228 / 1C / PRS 101 / PAO1) | 27% | 100% |
P53435 | Mycobacterium leprae (strain TN) | 29% | 100% |
P64183 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 30% | 100% |
P64185 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 29% | 100% |
P74257 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 30% | 100% |
P90795 | Caenorhabditis elegans | 36% | 84% |
P9WN78 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 29% | 100% |
P9WN79 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 29% | 100% |
P9WN80 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 30% | 100% |
P9WN81 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 30% | 100% |
Q2FHD8 | Staphylococcus aureus (strain USA300) | 31% | 100% |
Q2FYZ4 | Staphylococcus aureus (strain NCTC 8325 / PS 47) | 31% | 100% |
Q2YIQ2 | Brucella abortus (strain 2308) | 28% | 100% |
Q2YXR5 | Staphylococcus aureus (strain bovine RF122 / ET3-1) | 31% | 100% |
Q49X94 | Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM 20229 / NCIMB 8711 / NCTC 7292 / S-41) | 31% | 100% |
Q4L608 | Staphylococcus haemolyticus (strain JCSC1435) | 32% | 100% |
Q4R755 | Macaca fascicularis | 37% | 84% |
Q54QC1 | Dictyostelium discoideum | 34% | 95% |
Q5HGD1 | Staphylococcus aureus (strain COL) | 31% | 100% |
Q5HPP0 | Staphylococcus epidermidis (strain ATCC 35984 / RP62A) | 32% | 100% |
Q5XAK0 | Streptococcus pyogenes serotype M6 (strain ATCC BAA-946 / MGAS10394) | 27% | 99% |
Q64521 | Mus musculus | 37% | 84% |
Q6G9R2 | Staphylococcus aureus (strain MSSA476) | 31% | 100% |
Q6GHD4 | Staphylococcus aureus (strain MRSA252) | 31% | 100% |
Q7A105 | Staphylococcus aureus (strain MW2) | 31% | 100% |
Q7A5V7 | Staphylococcus aureus (strain N315) | 31% | 100% |
Q8CPE6 | Staphylococcus epidermidis (strain ATCC 12228 / FDA PCI 1200) | 32% | 100% |
Q8NZX0 | Streptococcus pyogenes serotype M18 (strain MGAS8232) | 27% | 99% |
Q8SR40 | Encephalitozoon cuniculi (strain GB-M1) | 33% | 99% |
Q99UH2 | Staphylococcus aureus (strain Mu50 / ATCC 700699) | 31% | 100% |
Q99YI8 | Streptococcus pyogenes serotype M1 | 27% | 99% |
Q9CG65 | Lactococcus lactis subsp. lactis (strain IL1403) | 26% | 100% |
Q9SS48 | Arabidopsis thaliana | 39% | 97% |
V5AUH1 | Trypanosoma cruzi | 56% | 88% |
V5BVH7 | Trypanosoma cruzi | 24% | 99% |