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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H8G7
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0019752 | carboxylic acid metabolic process | 5 | 10 |
GO:0043436 | oxoacid metabolic process | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044281 | small molecule metabolic process | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0016829 | lyase activity | 2 | 10 |
GO:0016830 | carbon-carbon lyase activity | 3 | 10 |
GO:0019842 | vitamin binding | 3 | 10 |
GO:0030170 | pyridoxal phosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0070279 | vitamin B6 binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0016831 | carboxy-lyase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 255 | 259 | PF00656 | 0.401 |
CLV_MEL_PAP_1 | 373 | 379 | PF00089 | 0.551 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.480 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.487 |
CLV_PCSK_KEX2_1 | 445 | 447 | PF00082 | 0.816 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 543 | 545 | PF00082 | 0.456 |
CLV_PCSK_PC1ET2_1 | 137 | 139 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 445 | 447 | PF00082 | 0.816 |
CLV_PCSK_PC1ET2_1 | 543 | 545 | PF00082 | 0.399 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 412 | 416 | PF00082 | 0.436 |
DEG_APCC_DBOX_1 | 384 | 392 | PF00400 | 0.525 |
DEG_COP1_1 | 255 | 266 | PF00400 | 0.427 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.526 |
DEG_SPOP_SBC_1 | 12 | 16 | PF00917 | 0.637 |
DEG_SPOP_SBC_1 | 530 | 534 | PF00917 | 0.427 |
DOC_CKS1_1 | 317 | 322 | PF01111 | 0.561 |
DOC_CKS1_1 | 439 | 444 | PF01111 | 0.513 |
DOC_CYCLIN_yCln2_LP_2 | 552 | 558 | PF00134 | 0.438 |
DOC_MAPK_DCC_7 | 475 | 483 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 492 | 500 | PF00069 | 0.448 |
DOC_MAPK_MEF2A_6 | 475 | 483 | PF00069 | 0.565 |
DOC_MAPK_MEF2A_6 | 492 | 500 | PF00069 | 0.375 |
DOC_MAPK_RevD_3 | 123 | 138 | PF00069 | 0.411 |
DOC_PP1_RVXF_1 | 295 | 302 | PF00149 | 0.377 |
DOC_PP2B_LxvP_1 | 140 | 143 | PF13499 | 0.597 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 252 | 256 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 368 | 372 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.623 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.633 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.751 |
LIG_14-3-3_CanoR_1 | 11 | 21 | PF00244 | 0.713 |
LIG_14-3-3_CanoR_1 | 129 | 135 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 2 | 10 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 310 | 315 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 364 | 373 | PF00244 | 0.609 |
LIG_14-3-3_CanoR_1 | 446 | 451 | PF00244 | 0.797 |
LIG_14-3-3_CanoR_1 | 475 | 479 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 554 | 563 | PF00244 | 0.495 |
LIG_CaM_IQ_9 | 75 | 90 | PF13499 | 0.355 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.555 |
LIG_FHA_1 | 22 | 28 | PF00498 | 0.553 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.560 |
LIG_FHA_1 | 344 | 350 | PF00498 | 0.548 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.473 |
LIG_FHA_1 | 534 | 540 | PF00498 | 0.531 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.423 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.373 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.491 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.582 |
LIG_FHA_2 | 413 | 419 | PF00498 | 0.467 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.518 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.502 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.494 |
LIG_Integrin_RGD_1 | 392 | 394 | PF01839 | 0.555 |
LIG_LIR_Gen_1 | 455 | 466 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 67 | 76 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 404 | 409 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 455 | 461 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 499 | 503 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.487 |
LIG_LYPXL_S_1 | 182 | 186 | PF13949 | 0.278 |
LIG_LYPXL_yS_3 | 183 | 186 | PF13949 | 0.278 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.570 |
LIG_SH2_CRK | 458 | 462 | PF00017 | 0.523 |
LIG_SH2_CRK | 69 | 73 | PF00017 | 0.470 |
LIG_SH2_NCK_1 | 251 | 255 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 163 | 167 | PF00017 | 0.345 |
LIG_SH2_STAP1 | 62 | 66 | PF00017 | 0.494 |
LIG_SH2_STAP1 | 69 | 73 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.526 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.586 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.446 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.385 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.702 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.498 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.471 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.452 |
LIG_SUMO_SIM_par_1 | 69 | 75 | PF11976 | 0.384 |
LIG_TYR_ITIM | 270 | 275 | PF00017 | 0.611 |
LIG_WRC_WIRS_1 | 188 | 193 | PF05994 | 0.394 |
MOD_CDK_SPxxK_3 | 438 | 445 | PF00069 | 0.515 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.629 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.567 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.400 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.593 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.522 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.507 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.758 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.647 |
MOD_CK1_1 | 464 | 470 | PF00069 | 0.573 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.497 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.640 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.441 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.590 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.504 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.472 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.425 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.584 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.765 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.539 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.546 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.676 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.518 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.475 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.505 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.575 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.464 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.619 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.552 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.400 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.425 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.645 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.714 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.589 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.457 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.512 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.644 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.777 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.533 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.438 |
MOD_N-GLC_1 | 461 | 466 | PF02516 | 0.513 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.601 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.618 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.370 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.513 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.442 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.369 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.468 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.626 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.556 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.491 |
MOD_Plk_1 | 397 | 403 | PF00069 | 0.485 |
MOD_Plk_1 | 418 | 424 | PF00069 | 0.597 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.533 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.374 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.447 |
MOD_Plk_4 | 401 | 407 | PF00069 | 0.500 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.610 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.402 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.574 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.564 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.504 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.636 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.748 |
TRG_DiLeu_BaLyEn_6 | 499 | 504 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.278 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.639 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.476 |
TRG_ER_diArg_1 | 492 | 494 | PF00400 | 0.482 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDL2 | Leptomonas seymouri | 47% | 76% |
A0A1X0P0L1 | Trypanosomatidae | 30% | 82% |
A0A3Q8IDL2 | Leishmania donovani | 76% | 99% |
A0A3R7K963 | Trypanosoma rangeli | 34% | 100% |
A4HWU0 | Leishmania infantum | 76% | 99% |
C9ZW41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 93% |
E9AQJ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 99% |
Q4QEX8 | Leishmania major | 76% | 100% |