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 |
Related structures:
AlphaFold database: E9AL32
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016491 | oxidoreductase activity | 2 | 1 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 357 | 361 | PF00656 | 0.723 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 582 | 584 | PF00675 | 0.437 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.524 |
CLV_Separin_Metazoa | 402 | 406 | PF03568 | 0.527 |
DEG_APCC_DBOX_1 | 20 | 28 | PF00400 | 0.670 |
DEG_SCF_FBW7_2 | 375 | 381 | PF00400 | 0.310 |
DOC_CDC14_PxL_1 | 422 | 430 | PF14671 | 0.495 |
DOC_CKS1_1 | 375 | 380 | PF01111 | 0.317 |
DOC_CYCLIN_RxL_1 | 505 | 513 | PF00134 | 0.557 |
DOC_MAPK_gen_1 | 228 | 236 | PF00069 | 0.662 |
DOC_MAPK_gen_1 | 525 | 533 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 9 | 17 | PF00069 | 0.650 |
DOC_MAPK_MEF2A_6 | 11 | 19 | PF00069 | 0.612 |
DOC_MAPK_MEF2A_6 | 228 | 236 | PF00069 | 0.615 |
DOC_MAPK_MEF2A_6 | 495 | 503 | PF00069 | 0.544 |
DOC_PP2B_LxvP_1 | 496 | 499 | PF13499 | 0.529 |
DOC_PP4_FxxP_1 | 432 | 435 | PF00568 | 0.395 |
DOC_PP4_FxxP_1 | 453 | 456 | PF00568 | 0.572 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.654 |
DOC_USP7_UBL2_3 | 71 | 75 | PF12436 | 0.792 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 374 | 379 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 617 | 622 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.758 |
LIG_14-3-3_CanoR_1 | 139 | 149 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 162 | 172 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 552 | 559 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 594 | 600 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 9 | 18 | PF00244 | 0.392 |
LIG_14-3-3_CterR_2 | 631 | 635 | PF00244 | 0.682 |
LIG_APCC_ABBA_1 | 385 | 390 | PF00400 | 0.478 |
LIG_BRCT_BRCA1_1 | 449 | 453 | PF00533 | 0.396 |
LIG_deltaCOP1_diTrp_1 | 568 | 575 | PF00928 | 0.433 |
LIG_eIF4E_1 | 388 | 394 | PF01652 | 0.474 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.388 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.429 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.525 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.440 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.481 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.529 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.467 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.438 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.514 |
LIG_FHA_1 | 609 | 615 | PF00498 | 0.481 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.759 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.450 |
LIG_LIR_Apic_2 | 430 | 435 | PF02991 | 0.390 |
LIG_LIR_Apic_2 | 450 | 456 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 290 | 299 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 318 | 329 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 366 | 375 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 398 | 409 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 290 | 294 | PF02991 | 0.574 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 318 | 324 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 366 | 371 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 424 | 428 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 490 | 494 | PF02991 | 0.609 |
LIG_LYPXL_yS_3 | 425 | 428 | PF13949 | 0.520 |
LIG_PCNA_yPIPBox_3 | 582 | 591 | PF02747 | 0.572 |
LIG_Pex14_1 | 160 | 164 | PF04695 | 0.681 |
LIG_SH2_CRK | 300 | 304 | PF00017 | 0.510 |
LIG_SH2_CRK | 321 | 325 | PF00017 | 0.483 |
LIG_SH2_CRK | 491 | 495 | PF00017 | 0.631 |
LIG_SH2_SRC | 291 | 294 | PF00017 | 0.551 |
LIG_SH2_STAP1 | 300 | 304 | PF00017 | 0.498 |
LIG_SH2_STAP1 | 321 | 325 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 388 | 392 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.735 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.630 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.535 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.433 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.508 |
LIG_SUMO_SIM_anti_2 | 12 | 19 | PF11976 | 0.609 |
LIG_TRAF2_1 | 445 | 448 | PF00917 | 0.550 |
LIG_TYR_ITIM | 319 | 324 | PF00017 | 0.521 |
LIG_TYR_ITIM | 423 | 428 | PF00017 | 0.518 |
LIG_TYR_ITSM | 296 | 303 | PF00017 | 0.518 |
LIG_UBA3_1 | 379 | 386 | PF00899 | 0.400 |
LIG_UBA3_1 | 517 | 525 | PF00899 | 0.555 |
LIG_WRC_WIRS_1 | 368 | 373 | PF05994 | 0.656 |
MOD_CDK_SPK_2 | 240 | 245 | PF00069 | 0.656 |
MOD_CDK_SPK_2 | 431 | 436 | PF00069 | 0.383 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.653 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.718 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.682 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.441 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.758 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.661 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.700 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.536 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.670 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.698 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.557 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.672 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.636 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.653 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.760 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.538 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.461 |
MOD_GlcNHglycan | 40 | 44 | PF01048 | 0.676 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.662 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.456 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.555 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.738 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.446 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.774 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.698 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.746 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.553 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.650 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.630 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.506 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.503 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.655 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.647 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.510 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.765 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.572 |
MOD_N-GLC_1 | 442 | 447 | PF02516 | 0.564 |
MOD_N-GLC_1 | 607 | 612 | PF02516 | 0.650 |
MOD_N-GLC_1 | 617 | 622 | PF02516 | 0.710 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.623 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.503 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.319 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.603 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.536 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.513 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.702 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.462 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.632 |
MOD_NEK2_2 | 315 | 320 | PF00069 | 0.446 |
MOD_PIKK_1 | 456 | 462 | PF00454 | 0.593 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.758 |
MOD_PKA_2 | 551 | 557 | PF00069 | 0.438 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.429 |
MOD_Plk_1 | 447 | 453 | PF00069 | 0.582 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.560 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.559 |
MOD_Plk_4 | 595 | 601 | PF00069 | 0.597 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.675 |
MOD_ProDKin_1 | 374 | 380 | PF00069 | 0.327 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.466 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.390 |
MOD_ProDKin_1 | 617 | 623 | PF00069 | 0.702 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.754 |
MOD_SUMO_rev_2 | 254 | 264 | PF00179 | 0.581 |
TRG_DiLeu_BaLyEn_6 | 375 | 380 | PF01217 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 453 | 458 | PF01217 | 0.471 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.551 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.522 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 491 | 494 | PF00928 | 0.606 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.675 |
TRG_ER_diArg_1 | 268 | 271 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 581 | 583 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.627 |
TRG_Pf-PMV_PEXEL_1 | 391 | 395 | PF00026 | 0.465 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7J6 | Leptomonas seymouri | 61% | 99% |
A0A3R7NMJ1 | Trypanosoma rangeli | 33% | 100% |
A0A3S5H5W7 | Leishmania donovani | 91% | 100% |
A4H4W6 | Leishmania braziliensis | 74% | 97% |
A4HT40 | Leishmania infantum | 91% | 100% |
C9ZUU8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
Q4QIS2 | Leishmania major | 91% | 100% |
V5B8V4 | Trypanosoma cruzi | 36% | 100% |