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: 6 |
Silverman et al. | yes | yes: 3 |
Pissara et al. | yes | yes: 30 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: Q4Q673
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 4 |
GO:0006807 | nitrogen compound metabolic process | 2 | 4 |
GO:0008152 | metabolic process | 1 | 4 |
GO:0019538 | protein metabolic process | 3 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 4 |
GO:0044238 | primary metabolic process | 2 | 4 |
GO:0071704 | organic substance metabolic process | 2 | 4 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 23 |
GO:0008233 | peptidase activity | 3 | 4 |
GO:0016787 | hydrolase activity | 2 | 23 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 4 |
GO:0005488 | binding | 1 | 1 |
GO:0005506 | iron ion binding | 6 | 1 |
GO:0016491 | oxidoreductase activity | 2 | 1 |
GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
GO:0046914 | transition metal ion binding | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 35 | 39 | PF00656 | 0.573 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.597 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 459 | 461 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 471 | 475 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.398 |
DEG_APCC_DBOX_1 | 346 | 354 | PF00400 | 0.384 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.556 |
DEG_SPOP_SBC_1 | 70 | 74 | PF00917 | 0.566 |
DOC_ANK_TNKS_1 | 211 | 218 | PF00023 | 0.475 |
DOC_ANK_TNKS_1 | 313 | 320 | PF00023 | 0.386 |
DOC_CYCLIN_RxL_1 | 344 | 354 | PF00134 | 0.372 |
DOC_CYCLIN_RxL_1 | 75 | 83 | PF00134 | 0.547 |
DOC_MAPK_FxFP_2 | 55 | 58 | PF00069 | 0.572 |
DOC_MAPK_gen_1 | 285 | 293 | PF00069 | 0.448 |
DOC_MAPK_gen_1 | 77 | 84 | PF00069 | 0.555 |
DOC_MAPK_MEF2A_6 | 181 | 189 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 287 | 295 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 434 | 443 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 77 | 84 | PF00069 | 0.555 |
DOC_MAPK_NFAT4_5 | 77 | 85 | PF00069 | 0.550 |
DOC_PP1_RVXF_1 | 469 | 475 | PF00149 | 0.413 |
DOC_PP2B_LxvP_1 | 30 | 33 | PF13499 | 0.562 |
DOC_PP2B_LxvP_1 | 551 | 554 | PF13499 | 0.370 |
DOC_PP4_FxxP_1 | 411 | 414 | PF00568 | 0.448 |
DOC_PP4_FxxP_1 | 55 | 58 | PF00568 | 0.572 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.573 |
DOC_USP7_UBL2_3 | 471 | 475 | PF12436 | 0.518 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.478 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.474 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 571 | 576 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.508 |
LIG_14-3-3_CanoR_1 | 114 | 118 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 434 | 440 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 77 | 81 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 87 | 97 | PF00244 | 0.512 |
LIG_APCC_ABBA_1 | 524 | 529 | PF00400 | 0.386 |
LIG_BRCT_BRCA1_1 | 138 | 142 | PF00533 | 0.572 |
LIG_EH1_1 | 531 | 539 | PF00400 | 0.399 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.552 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.448 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.388 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.436 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.322 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.415 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.388 |
LIG_FHA_1 | 558 | 564 | PF00498 | 0.392 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.400 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.580 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.517 |
LIG_FHA_2 | 89 | 95 | PF00498 | 0.549 |
LIG_LIR_Apic_2 | 52 | 58 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 130 | 140 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 172 | 178 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 182 | 190 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 237 | 248 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 301 | 309 | PF02991 | 0.386 |
LIG_LIR_Gen_1 | 549 | 556 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 98 | 108 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 107 | 113 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 172 | 176 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 182 | 187 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 237 | 243 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 549 | 553 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 98 | 103 | PF02991 | 0.621 |
LIG_LRP6_Inhibitor_1 | 428 | 434 | PF00058 | 0.471 |
LIG_MYND_1 | 209 | 213 | PF01753 | 0.388 |
LIG_MYND_1 | 486 | 490 | PF01753 | 0.400 |
LIG_Pex14_2 | 142 | 146 | PF04695 | 0.601 |
LIG_Pex14_2 | 386 | 390 | PF04695 | 0.413 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.482 |
LIG_SH2_PTP2 | 132 | 135 | PF00017 | 0.467 |
LIG_SH2_SRC | 132 | 135 | PF00017 | 0.480 |
LIG_SH2_SRC | 173 | 176 | PF00017 | 0.402 |
LIG_SH2_STAP1 | 240 | 244 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 304 | 308 | PF00017 | 0.400 |
LIG_SH2_STAT3 | 508 | 511 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 41 | 44 | PF00017 | 0.595 |
LIG_SH3_1 | 207 | 213 | PF00018 | 0.388 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.574 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.397 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.437 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.573 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.559 |
LIG_SH3_3 | 93 | 99 | PF00018 | 0.498 |
LIG_SH3_4 | 489 | 496 | PF00018 | 0.299 |
LIG_SH3_5 | 275 | 279 | PF00018 | 0.442 |
LIG_SUMO_SIM_par_1 | 262 | 267 | PF11976 | 0.390 |
LIG_TRAF2_1 | 268 | 271 | PF00917 | 0.384 |
LIG_TYR_ITIM | 171 | 176 | PF00017 | 0.510 |
LIG_UBA3_1 | 349 | 357 | PF00899 | 0.464 |
LIG_WRC_WIRS_1 | 100 | 105 | PF05994 | 0.467 |
MOD_CDC14_SPxK_1 | 17 | 20 | PF00782 | 0.568 |
MOD_CDC14_SPxK_1 | 21 | 24 | PF00782 | 0.568 |
MOD_CDC14_SPxK_1 | 74 | 77 | PF00782 | 0.557 |
MOD_CDK_SPK_2 | 571 | 576 | PF00069 | 0.505 |
MOD_CDK_SPxK_1 | 14 | 20 | PF00069 | 0.574 |
MOD_CDK_SPxK_1 | 71 | 77 | PF00069 | 0.564 |
MOD_CDK_SPxxK_3 | 71 | 78 | PF00069 | 0.559 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.583 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.428 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.400 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.524 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.454 |
MOD_DYRK1A_RPxSP_1 | 95 | 99 | PF00069 | 0.507 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.572 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.514 |
MOD_GlcNHglycan | 270 | 274 | PF01048 | 0.402 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.382 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.392 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.563 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.580 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.544 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.463 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.529 |
MOD_GSK3_1 | 339 | 346 | PF00069 | 0.444 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.428 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.541 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.409 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.590 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.690 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.491 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.395 |
MOD_N-GLC_1 | 302 | 307 | PF02516 | 0.505 |
MOD_N-GLC_2 | 481 | 483 | PF02516 | 0.469 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.428 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.369 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.412 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.471 |
MOD_NEK2_1 | 504 | 509 | PF00069 | 0.424 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.422 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.485 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.480 |
MOD_PIKK_1 | 47 | 53 | PF00454 | 0.560 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.477 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.520 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.587 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.475 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.443 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.505 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.460 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.386 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.468 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.481 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.482 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.574 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.455 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.563 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.474 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.559 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.526 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.564 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.506 |
MOD_SUMO_for_1 | 449 | 452 | PF00179 | 0.386 |
MOD_SUMO_rev_2 | 351 | 358 | PF00179 | 0.448 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.400 |
TRG_NES_CRM1_1 | 286 | 298 | PF08389 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 460 | 465 | PF00026 | 0.431 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1Q9 | Leptomonas seymouri | 75% | 100% |
A0A0N1PBD8 | Leptomonas seymouri | 78% | 100% |
A0A0S4JJE7 | Bodo saltans | 60% | 100% |
A0A1X0P1Q0 | Trypanosomatidae | 64% | 100% |
A0A381MQ29 | Leishmania infantum | 98% | 100% |
A0A3Q8IFP2 | Leishmania donovani | 95% | 100% |
A0A3R7KSZ4 | Trypanosoma rangeli | 63% | 100% |
A0A3S7X4P6 | Leishmania donovani | 97% | 100% |
A0A3S7X6U2 | Leishmania donovani | 75% | 100% |
A4HJG9 | Leishmania braziliensis | 92% | 100% |
A4HJH1 | Leishmania braziliensis | 92% | 100% |
A4HJI4 | Leishmania braziliensis | 92% | 100% |
A4HLM2 | Leishmania braziliensis | 72% | 100% |
A4I933 | Leishmania infantum | 75% | 100% |
C9ZQ48 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
D0A536 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9B201 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9B3Z8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4Q426 | Leishmania major | 74% | 100% |
Q4Q660 | Leishmania major | 100% | 100% |
Q6Q0N1 | Rattus norvegicus | 27% | 100% |
Q9D1A2 | Mus musculus | 27% | 100% |
V5BHA2 | Trypanosoma cruzi | 62% | 100% |