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:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0005576 | extracellular region | 2 | 4 |
Related structures:
AlphaFold database: A4HPY1
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0008233 | peptidase activity | 3 | 2 |
GO:0008236 | serine-type peptidase activity | 4 | 2 |
GO:0016787 | hydrolase activity | 2 | 6 |
GO:0017171 | serine hydrolase activity | 3 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
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 | 149 | 153 | PF00656 | 0.339 |
CLV_C14_Caspase3-7 | 416 | 420 | PF00656 | 0.467 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.691 |
CLV_NRD_NRD_1 | 435 | 437 | PF00675 | 0.807 |
CLV_NRD_NRD_1 | 497 | 499 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 509 | 511 | PF00675 | 0.711 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.768 |
CLV_PCSK_KEX2_1 | 453 | 455 | PF00082 | 0.766 |
CLV_PCSK_KEX2_1 | 497 | 499 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.711 |
CLV_PCSK_PC1ET2_1 | 453 | 455 | PF00082 | 0.761 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 435 | 439 | PF00082 | 0.875 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.713 |
CLV_Separin_Metazoa | 552 | 556 | PF03568 | 0.407 |
DEG_APCC_DBOX_1 | 40 | 48 | PF00400 | 0.433 |
DEG_APCC_DBOX_1 | 420 | 428 | PF00400 | 0.465 |
DEG_APCC_KENBOX_2 | 131 | 135 | PF00400 | 0.324 |
DEG_SPOP_SBC_1 | 296 | 300 | PF00917 | 0.311 |
DOC_CYCLIN_yCln2_LP_2 | 114 | 120 | PF00134 | 0.332 |
DOC_CYCLIN_yCln2_LP_2 | 52 | 58 | PF00134 | 0.415 |
DOC_MAPK_gen_1 | 121 | 129 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 154 | 164 | PF00069 | 0.280 |
DOC_MAPK_gen_1 | 39 | 47 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 415 | 424 | PF00069 | 0.467 |
DOC_MAPK_HePTP_8 | 151 | 163 | PF00069 | 0.299 |
DOC_MAPK_MEF2A_6 | 154 | 163 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 39 | 46 | PF00069 | 0.433 |
DOC_MAPK_NFAT4_5 | 39 | 47 | PF00069 | 0.433 |
DOC_MAPK_RevD_3 | 83 | 98 | PF00069 | 0.290 |
DOC_PP1_RVXF_1 | 319 | 326 | PF00149 | 0.397 |
DOC_PP2B_LxvP_1 | 114 | 117 | PF13499 | 0.348 |
DOC_PP2B_LxvP_1 | 141 | 144 | PF13499 | 0.268 |
DOC_PP2B_LxvP_1 | 52 | 55 | PF13499 | 0.415 |
DOC_USP7_MATH_1 | 395 | 399 | PF00917 | 0.467 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.356 |
DOC_USP7_UBL2_3 | 449 | 453 | PF12436 | 0.563 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 515 | 520 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.401 |
LIG_14-3-3_CanoR_1 | 123 | 127 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 267 | 273 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 301 | 305 | PF00244 | 0.396 |
LIG_14-3-3_CanoR_1 | 35 | 43 | PF00244 | 0.638 |
LIG_14-3-3_CanoR_1 | 434 | 440 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 481 | 486 | PF00244 | 0.477 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.641 |
LIG_BIR_III_4 | 177 | 181 | PF00653 | 0.331 |
LIG_BRCT_BRCA1_1 | 381 | 385 | PF00533 | 0.448 |
LIG_BRCT_BRCA1_1 | 485 | 489 | PF00533 | 0.541 |
LIG_Clathr_ClatBox_1 | 553 | 557 | PF01394 | 0.297 |
LIG_EH1_1 | 82 | 90 | PF00400 | 0.419 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.250 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.454 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.288 |
LIG_FHA_1 | 570 | 576 | PF00498 | 0.368 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.366 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.333 |
LIG_FHA_2 | 361 | 367 | PF00498 | 0.401 |
LIG_GBD_Chelix_1 | 228 | 236 | PF00786 | 0.433 |
LIG_LIR_Gen_1 | 351 | 360 | PF02991 | 0.433 |
LIG_LIR_Gen_1 | 523 | 528 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 179 | 184 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 523 | 527 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 61 | 65 | PF02991 | 0.354 |
LIG_PTB_Apo_2 | 353 | 360 | PF02174 | 0.408 |
LIG_PTB_Phospho_1 | 353 | 359 | PF10480 | 0.405 |
LIG_Rb_LxCxE_1 | 255 | 271 | PF01857 | 0.233 |
LIG_SH2_GRB2like | 354 | 357 | PF00017 | 0.406 |
LIG_SH2_GRB2like | 461 | 464 | PF00017 | 0.460 |
LIG_SH2_NCK_1 | 461 | 465 | PF00017 | 0.461 |
LIG_SH2_SRC | 461 | 464 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 354 | 358 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 43 | 46 | PF00017 | 0.292 |
LIG_SH2_STAT5 | 511 | 514 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.528 |
LIG_SH2_STAT5 | 574 | 577 | PF00017 | 0.421 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.449 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.307 |
LIG_SH3_3 | 407 | 413 | PF00018 | 0.462 |
LIG_SUMO_SIM_anti_2 | 549 | 555 | PF11976 | 0.410 |
LIG_TRAF2_1 | 2 | 5 | PF00917 | 0.675 |
LIG_TRAF2_1 | 429 | 432 | PF00917 | 0.470 |
LIG_UBA3_1 | 164 | 173 | PF00899 | 0.371 |
LIG_UBA3_1 | 88 | 97 | PF00899 | 0.284 |
LIG_WRC_WIRS_1 | 126 | 131 | PF05994 | 0.402 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.434 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.297 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.609 |
MOD_CK1_1 | 350 | 356 | PF00069 | 0.412 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.489 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.409 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.411 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.472 |
MOD_CK2_1 | 546 | 552 | PF00069 | 0.506 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.346 |
MOD_Cter_Amidation | 432 | 435 | PF01082 | 0.676 |
MOD_Cter_Amidation | 95 | 98 | PF01082 | 0.495 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.398 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.672 |
MOD_GlcNHglycan | 426 | 430 | PF01048 | 0.664 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.753 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.523 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.365 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.307 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.324 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.409 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.626 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.450 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.537 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.403 |
MOD_N-GLC_1 | 481 | 486 | PF02516 | 0.692 |
MOD_N-GLC_1 | 520 | 525 | PF02516 | 0.647 |
MOD_N-GLC_2 | 339 | 341 | PF02516 | 0.618 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.378 |
MOD_NEK2_1 | 191 | 196 | PF00069 | 0.243 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.391 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.483 |
MOD_PIKK_1 | 427 | 433 | PF00454 | 0.467 |
MOD_PIKK_1 | 435 | 441 | PF00454 | 0.464 |
MOD_PIKK_1 | 546 | 552 | PF00454 | 0.431 |
MOD_PKA_1 | 435 | 441 | PF00069 | 0.558 |
MOD_PKA_1 | 509 | 515 | PF00069 | 0.443 |
MOD_PKA_2 | 122 | 128 | PF00069 | 0.284 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.395 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.623 |
MOD_PKA_2 | 435 | 441 | PF00069 | 0.570 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.443 |
MOD_PKB_1 | 415 | 423 | PF00069 | 0.518 |
MOD_PKB_1 | 481 | 489 | PF00069 | 0.476 |
MOD_Plk_1 | 481 | 487 | PF00069 | 0.477 |
MOD_Plk_1 | 520 | 526 | PF00069 | 0.445 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.400 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.395 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.455 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.422 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.467 |
MOD_ProDKin_1 | 515 | 521 | PF00069 | 0.448 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.406 |
MOD_SUMO_for_1 | 385 | 388 | PF00179 | 0.453 |
MOD_SUMO_rev_2 | 343 | 348 | PF00179 | 0.352 |
TRG_ENDOCYTIC_2 | 354 | 357 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.246 |
TRG_ER_diArg_1 | 156 | 158 | PF00400 | 0.298 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 508 | 510 | PF00400 | 0.502 |
TRG_Pf-PMV_PEXEL_1 | 23 | 27 | PF00026 | 0.424 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7XBJ7 | Leishmania donovani | 56% | 100% |
A4IDP2 | Leishmania infantum | 56% | 100% |
E9ATP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 56% | 100% |
Q4Q0V0 | Leishmania major | 57% | 99% |