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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005576 | extracellular region | 2 | 5 |
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: E9ATP8
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0016787 | hydrolase activity | 2 | 6 |
GO:0008233 | peptidase activity | 3 | 1 |
GO:0008236 | serine-type peptidase activity | 4 | 1 |
GO:0017171 | serine hydrolase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0030600 | feruloyl esterase activity | 5 | 1 |
GO:0052689 | carboxylic ester hydrolase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 399 | 403 | PF00656 | 0.429 |
CLV_C14_Caspase3-7 | 475 | 479 | PF00656 | 0.443 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 417 | 419 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.724 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 444 | 446 | PF00675 | 0.654 |
CLV_NRD_NRD_1 | 515 | 517 | PF00675 | 0.764 |
CLV_PCSK_FUR_1 | 415 | 419 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 417 | 419 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 444 | 446 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 515 | 517 | PF00082 | 0.764 |
CLV_PCSK_PC7_1 | 430 | 436 | PF00082 | 0.721 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.767 |
CLV_Separin_Metazoa | 550 | 554 | PF03568 | 0.456 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.597 |
DOC_CKS1_1 | 75 | 80 | PF01111 | 0.426 |
DOC_CYCLIN_yCln2_LP_2 | 52 | 58 | PF00134 | 0.473 |
DOC_MAPK_gen_1 | 121 | 129 | PF00069 | 0.447 |
DOC_MAPK_gen_1 | 515 | 522 | PF00069 | 0.562 |
DOC_MAPK_gen_1 | 527 | 534 | PF00069 | 0.482 |
DOC_MAPK_JIP1_4 | 157 | 163 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 157 | 165 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 187 | 195 | PF00069 | 0.221 |
DOC_PP2B_LxvP_1 | 26 | 29 | PF13499 | 0.740 |
DOC_PP2B_LxvP_1 | 52 | 55 | PF13499 | 0.491 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.352 |
DOC_USP7_UBL2_3 | 463 | 467 | PF12436 | 0.565 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.352 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 536 | 541 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.476 |
LIG_14-3-3_CanoR_1 | 267 | 273 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 301 | 305 | PF00244 | 0.395 |
LIG_BIR_III_2 | 155 | 159 | PF00653 | 0.221 |
LIG_BIR_III_4 | 177 | 181 | PF00653 | 0.330 |
LIG_BRCT_BRCA1_1 | 485 | 489 | PF00533 | 0.554 |
LIG_BRCT_BRCA1_1 | 79 | 83 | PF00533 | 0.481 |
LIG_EH1_1 | 82 | 90 | PF00400 | 0.465 |
LIG_eIF4E_1 | 390 | 396 | PF01652 | 0.421 |
LIG_EVH1_2 | 381 | 385 | PF00568 | 0.421 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.395 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.278 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.475 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.221 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.469 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.550 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.436 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.504 |
LIG_LIR_Apic_2 | 145 | 150 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 188 | 195 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 128 | 132 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 179 | 184 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 188 | 193 | PF02991 | 0.248 |
LIG_NRBOX | 516 | 522 | PF00104 | 0.431 |
LIG_PCNA_yPIPBox_3 | 82 | 90 | PF02747 | 0.422 |
LIG_PTB_Apo_2 | 353 | 360 | PF02174 | 0.440 |
LIG_PTB_Phospho_1 | 353 | 359 | PF10480 | 0.438 |
LIG_SH2_GRB2like | 354 | 357 | PF00017 | 0.437 |
LIG_SH2_STAP1 | 359 | 363 | PF00017 | 0.283 |
LIG_SH2_STAP1 | 572 | 576 | PF00017 | 0.255 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.472 |
LIG_SH3_1 | 114 | 120 | PF00018 | 0.464 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.508 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.388 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.265 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.465 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.403 |
LIG_SUMO_SIM_anti_2 | 547 | 553 | PF11976 | 0.454 |
LIG_SUMO_SIM_anti_2 | 69 | 77 | PF11976 | 0.467 |
LIG_TRAF2_1 | 501 | 504 | PF00917 | 0.518 |
LIG_TRAF2_1 | 67 | 70 | PF00917 | 0.371 |
LIG_TRFH_1 | 489 | 493 | PF08558 | 0.741 |
LIG_UBA3_1 | 164 | 173 | PF00899 | 0.473 |
LIG_WRC_WIRS_1 | 126 | 131 | PF05994 | 0.547 |
LIG_WW_3 | 28 | 32 | PF00397 | 0.669 |
MOD_CDK_SPK_2 | 536 | 541 | PF00069 | 0.529 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.565 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.677 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.609 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.551 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.275 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.535 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.679 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.230 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.693 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.712 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.501 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.625 |
MOD_CK2_1 | 479 | 485 | PF00069 | 0.535 |
MOD_CK2_1 | 544 | 550 | PF00069 | 0.613 |
MOD_DYRK1A_RPxSP_1 | 367 | 371 | PF00069 | 0.499 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.412 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.619 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.546 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.343 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.342 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.479 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.501 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.664 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.626 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.647 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.296 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.673 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.578 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.544 |
MOD_N-GLC_1 | 397 | 402 | PF02516 | 0.700 |
MOD_N-GLC_1 | 479 | 484 | PF02516 | 0.589 |
MOD_N-GLC_2 | 339 | 341 | PF02516 | 0.473 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.501 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.473 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.525 |
MOD_NEK2_2 | 296 | 301 | PF00069 | 0.321 |
MOD_NEK2_2 | 354 | 359 | PF00069 | 0.376 |
MOD_PIKK_1 | 131 | 137 | PF00454 | 0.342 |
MOD_PIKK_1 | 499 | 505 | PF00454 | 0.738 |
MOD_PKA_1 | 31 | 37 | PF00069 | 0.636 |
MOD_PKA_1 | 430 | 436 | PF00069 | 0.604 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.473 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.659 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.585 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.533 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.412 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.504 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.491 |
MOD_Plk_1 | 570 | 576 | PF00069 | 0.284 |
MOD_Plk_1 | 69 | 75 | PF00069 | 0.399 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.582 |
MOD_Plk_2-3 | 544 | 550 | PF00069 | 0.354 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.542 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.603 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.473 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.412 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.436 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.600 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.426 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.565 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.483 |
MOD_ProDKin_1 | 536 | 542 | PF00069 | 0.526 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.591 |
MOD_SUMO_for_1 | 440 | 443 | PF00179 | 0.475 |
MOD_SUMO_rev_2 | 149 | 159 | PF00179 | 0.370 |
MOD_SUMO_rev_2 | 464 | 473 | PF00179 | 0.691 |
MOD_SUMO_rev_2 | 479 | 489 | PF00179 | 0.580 |
TRG_DiLeu_BaEn_1 | 432 | 437 | PF01217 | 0.467 |
TRG_DiLeu_BaEn_2 | 185 | 191 | PF01217 | 0.412 |
TRG_ER_diArg_1 | 365 | 367 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 417 | 419 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 429 | 431 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 444 | 447 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 515 | 517 | PF00400 | 0.736 |
TRG_Pf-PMV_PEXEL_1 | 90 | 94 | PF00026 | 0.437 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XBJ7 | Leishmania donovani | 80% | 100% |
A4HPY1 | Leishmania braziliensis | 56% | 100% |
A4IDP2 | Leishmania infantum | 79% | 100% |
Q4Q0V0 | Leishmania major | 75% | 99% |