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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HIG7
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0019752 | carboxylic acid metabolic process | 5 | 11 |
GO:0043436 | oxoacid metabolic process | 4 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044281 | small molecule metabolic process | 2 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0006066 | alcohol metabolic process | 3 | 1 |
GO:0006576 | biogenic amine metabolic process | 5 | 1 |
GO:0006580 | ethanolamine metabolic process | 5 | 1 |
GO:0006629 | lipid metabolic process | 3 | 1 |
GO:0006643 | membrane lipid metabolic process | 4 | 1 |
GO:0006665 | sphingolipid metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009308 | amine metabolic process | 4 | 1 |
GO:0009309 | amine biosynthetic process | 5 | 1 |
GO:0016042 | lipid catabolic process | 4 | 1 |
GO:0030149 | sphingolipid catabolic process | 5 | 1 |
GO:0034308 | primary alcohol metabolic process | 4 | 1 |
GO:0034309 | primary alcohol biosynthetic process | 5 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0042401 | biogenic amine biosynthetic process | 6 | 1 |
GO:0042439 | ethanolamine-containing compound metabolic process | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044242 | cellular lipid catabolic process | 4 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044255 | cellular lipid metabolic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0044283 | small molecule biosynthetic process | 3 | 1 |
GO:0046165 | alcohol biosynthetic process | 4 | 1 |
GO:0046335 | ethanolamine biosynthetic process | 6 | 1 |
GO:0046466 | membrane lipid catabolic process | 5 | 1 |
GO:1901160 | primary amino compound metabolic process | 4 | 1 |
GO:1901162 | primary amino compound biosynthetic process | 5 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 1 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
GO:1901615 | organic hydroxy compound metabolic process | 3 | 1 |
GO:1901617 | organic hydroxy compound biosynthetic process | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 11 |
GO:0008117 | sphinganine-1-phosphate aldolase activity | 5 | 8 |
GO:0016829 | lyase activity | 2 | 12 |
GO:0016830 | carbon-carbon lyase activity | 3 | 11 |
GO:0016832 | aldehyde-lyase activity | 4 | 8 |
GO:0019842 | vitamin binding | 3 | 11 |
GO:0030170 | pyridoxal phosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0070279 | vitamin B6 binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.192 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.513 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.393 |
CLV_PCSK_PC1ET2_1 | 45 | 47 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 524 | 528 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.449 |
DEG_SPOP_SBC_1 | 428 | 432 | PF00917 | 0.228 |
DOC_CDC14_PxL_1 | 232 | 240 | PF14671 | 0.419 |
DOC_CKS1_1 | 466 | 471 | PF01111 | 0.480 |
DOC_CYCLIN_yClb1_LxF_4 | 450 | 455 | PF00134 | 0.281 |
DOC_MAPK_gen_1 | 251 | 260 | PF00069 | 0.298 |
DOC_MAPK_gen_1 | 305 | 315 | PF00069 | 0.414 |
DOC_MAPK_gen_1 | 411 | 418 | PF00069 | 0.419 |
DOC_MAPK_gen_1 | 64 | 73 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 308 | 315 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 411 | 418 | PF00069 | 0.402 |
DOC_PP1_RVXF_1 | 450 | 456 | PF00149 | 0.293 |
DOC_PP2B_LxvP_1 | 86 | 89 | PF13499 | 0.590 |
DOC_PP2B_PxIxI_1 | 413 | 419 | PF00149 | 0.298 |
DOC_PP4_FxxP_1 | 298 | 301 | PF00568 | 0.282 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.206 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.287 |
DOC_USP7_MATH_1 | 428 | 432 | PF00917 | 0.313 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.496 |
DOC_USP7_MATH_2 | 89 | 95 | PF00917 | 0.435 |
DOC_USP7_UBL2_3 | 247 | 251 | PF12436 | 0.322 |
DOC_USP7_UBL2_3 | 65 | 69 | PF12436 | 0.441 |
DOC_USP7_UBL2_3 | 75 | 79 | PF12436 | 0.513 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 362 | 367 | PF00397 | 0.298 |
DOC_WW_Pin1_4 | 465 | 470 | PF00397 | 0.469 |
LIG_14-3-3_CanoR_1 | 53 | 59 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 68 | 74 | PF00244 | 0.564 |
LIG_APCC_ABBA_1 | 287 | 292 | PF00400 | 0.298 |
LIG_APCC_ABBA_1 | 299 | 304 | PF00400 | 0.298 |
LIG_BIR_III_4 | 176 | 180 | PF00653 | 0.298 |
LIG_BRCT_BRCA1_1 | 147 | 151 | PF00533 | 0.342 |
LIG_BRCT_BRCA1_1 | 348 | 352 | PF00533 | 0.298 |
LIG_eIF4E_1 | 227 | 233 | PF01652 | 0.282 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.246 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.466 |
LIG_FHA_1 | 184 | 190 | PF00498 | 0.282 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.282 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.296 |
LIG_FHA_1 | 255 | 261 | PF00498 | 0.228 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.288 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.284 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.282 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.396 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.393 |
LIG_GBD_Chelix_1 | 101 | 109 | PF00786 | 0.463 |
LIG_LIR_Gen_1 | 127 | 137 | PF02991 | 0.192 |
LIG_LIR_Gen_1 | 349 | 359 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 380 | 387 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 47 | 55 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 127 | 132 | PF02991 | 0.192 |
LIG_LIR_Nem_3 | 226 | 230 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.572 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.548 |
LIG_MYND_3 | 300 | 304 | PF01753 | 0.414 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.558 |
LIG_PDZ_Class_2 | 532 | 537 | PF00595 | 0.509 |
LIG_Pex14_2 | 298 | 302 | PF04695 | 0.282 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.454 |
LIG_SH2_CRK | 255 | 259 | PF00017 | 0.318 |
LIG_SH2_CRK | 363 | 367 | PF00017 | 0.298 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.333 |
LIG_SH2_GRB2like | 227 | 230 | PF00017 | 0.313 |
LIG_SH2_GRB2like | 7 | 10 | PF00017 | 0.541 |
LIG_SH2_NCK_1 | 255 | 259 | PF00017 | 0.318 |
LIG_SH2_PTP2 | 415 | 418 | PF00017 | 0.318 |
LIG_SH2_SRC | 113 | 116 | PF00017 | 0.398 |
LIG_SH2_STAP1 | 129 | 133 | PF00017 | 0.192 |
LIG_SH2_STAP1 | 255 | 259 | PF00017 | 0.342 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.192 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 252 | 255 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.562 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.418 |
LIG_SH3_3 | 262 | 268 | PF00018 | 0.286 |
LIG_SUMO_SIM_anti_2 | 18 | 24 | PF11976 | 0.451 |
LIG_SUMO_SIM_anti_2 | 462 | 468 | PF11976 | 0.322 |
LIG_SUMO_SIM_par_1 | 18 | 24 | PF11976 | 0.511 |
LIG_TRAF2_1 | 112 | 115 | PF00917 | 0.295 |
LIG_TRAF2_1 | 274 | 277 | PF00917 | 0.373 |
LIG_TYR_ITIM | 253 | 258 | PF00017 | 0.318 |
LIG_TYR_ITIM | 413 | 418 | PF00017 | 0.318 |
LIG_UBA3_1 | 189 | 194 | PF00899 | 0.318 |
LIG_UBA3_1 | 299 | 305 | PF00899 | 0.364 |
LIG_UBA3_1 | 436 | 444 | PF00899 | 0.415 |
LIG_WRC_WIRS_1 | 347 | 352 | PF05994 | 0.342 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.282 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.292 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.552 |
MOD_CK2_1 | 109 | 115 | PF00069 | 0.470 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.229 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.433 |
MOD_Cter_Amidation | 199 | 202 | PF01082 | 0.347 |
MOD_Cter_Amidation | 497 | 500 | PF01082 | 0.515 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.339 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.282 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.286 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.301 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.282 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.292 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.324 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.471 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.275 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.304 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.298 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.423 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.418 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.451 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.297 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.546 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.221 |
MOD_NEK2_2 | 422 | 427 | PF00069 | 0.298 |
MOD_PIKK_1 | 100 | 106 | PF00454 | 0.515 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.433 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.514 |
MOD_PK_1 | 69 | 75 | PF00069 | 0.421 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.359 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.377 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.494 |
MOD_PKB_1 | 316 | 324 | PF00069 | 0.373 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.474 |
MOD_Plk_2-3 | 91 | 97 | PF00069 | 0.427 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.276 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.298 |
MOD_Plk_4 | 185 | 191 | PF00069 | 0.298 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.292 |
MOD_Plk_4 | 336 | 342 | PF00069 | 0.283 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.298 |
MOD_Plk_4 | 461 | 467 | PF00069 | 0.301 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.462 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.454 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.417 |
MOD_Plk_4 | 530 | 536 | PF00069 | 0.504 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.564 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.480 |
MOD_ProDKin_1 | 362 | 368 | PF00069 | 0.298 |
MOD_ProDKin_1 | 465 | 471 | PF00069 | 0.475 |
MOD_SUMO_rev_2 | 240 | 249 | PF00179 | 0.204 |
MOD_SUMO_rev_2 | 78 | 86 | PF00179 | 0.450 |
TRG_DiLeu_BaEn_1 | 490 | 495 | PF01217 | 0.506 |
TRG_DiLeu_BaEn_1 | 97 | 102 | PF01217 | 0.447 |
TRG_DiLeu_BaEn_2 | 432 | 438 | PF01217 | 0.236 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.192 |
TRG_ENDOCYTIC_2 | 227 | 230 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.301 |
TRG_ENDOCYTIC_2 | 415 | 418 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.476 |
TRG_ER_diArg_1 | 315 | 318 | PF00400 | 0.373 |
TRG_NES_CRM1_1 | 100 | 115 | PF08389 | 0.512 |
TRG_Pf-PMV_PEXEL_1 | 417 | 421 | PF00026 | 0.384 |
TRG_Pf-PMV_PEXEL_1 | 475 | 479 | PF00026 | 0.361 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IBN8 | Leptomonas seymouri | 77% | 99% |
A0A0S4JRW4 | Bodo saltans | 54% | 99% |
A0A1X0P362 | Trypanosomatidae | 64% | 100% |
A0A3Q8IS31 | Leishmania donovani | 88% | 100% |
A0A3R7KL89 | Trypanosoma rangeli | 62% | 100% |
A4I5R3 | Leishmania infantum | 88% | 100% |
A5ULW4 | Methanobrevibacter smithii (strain ATCC 35061 / DSM 861 / OCM 144 / PS) | 28% | 100% |
A6UVR4 | Methanococcus aeolicus (strain ATCC BAA-1280 / DSM 17508 / OCM 812 / Nankai-3) | 28% | 100% |
C9ZR31 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9B108 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
O27188 | Methanothermobacter thermautotrophicus (strain ATCC 29096 / DSM 1053 / JCM 10044 / NBRC 100330 / Delta H) | 29% | 100% |
O58679 | Pyrococcus horikoshii (strain ATCC 700860 / DSM 12428 / JCM 9974 / NBRC 100139 / OT-3) | 28% | 100% |
O95470 | Homo sapiens | 39% | 95% |
Q05567 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 38% | 91% |
Q07346 | Petunia hybrida | 23% | 100% |
Q12VA2 | Methanococcoides burtonii (strain DSM 6242 / NBRC 107633 / OCM 468 / ACE-M) | 26% | 100% |
Q2NHY7 | Methanosphaera stadtmanae (strain ATCC 43021 / DSM 3091 / JCM 11832 / MCB-3) | 26% | 100% |
Q42472 | Arabidopsis thaliana | 24% | 100% |
Q4Q758 | Leishmania major | 85% | 100% |
Q52RG7 | Oryza sativa subsp. japonica | 41% | 100% |
Q54RV9 | Dictyostelium discoideum | 37% | 100% |
Q5R4G0 | Pongo abelii | 38% | 95% |
Q5WUR6 | Legionella pneumophila (strain Lens) | 35% | 89% |
Q5X3A8 | Legionella pneumophila (strain Paris) | 34% | 89% |
Q5ZTI6 | Legionella pneumophila subsp. pneumophila (strain Philadelphia 1 / ATCC 33152 / DSM 7513) | 33% | 89% |
Q8CHN6 | Rattus norvegicus | 40% | 95% |
Q8R0X7 | Mus musculus | 40% | 95% |
Q8U1P6 | Pyrococcus furiosus (strain ATCC 43587 / DSM 3638 / JCM 8422 / Vc1) | 28% | 100% |
Q9C509 | Arabidopsis thaliana | 42% | 99% |
Q9UZD5 | Pyrococcus abyssi (strain GE5 / Orsay) | 28% | 100% |
Q9V7Y2 | Drosophila melanogaster | 38% | 99% |
Q9Y194 | Caenorhabditis elegans | 36% | 97% |
Q9ZPS3 | Arabidopsis thaliana | 24% | 100% |
V5AWV1 | Trypanosoma cruzi | 61% | 86% |