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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WZZ0
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016491 | oxidoreductase activity | 2 | 7 |
GO:0004032 | alditol:NADP+ 1-oxidoreductase activity | 7 | 1 |
GO:0004033 | aldo-keto reductase (NADP) activity | 5 | 1 |
GO:0008106 | alcohol dehydrogenase (NADP+) activity | 6 | 1 |
GO:0016614 | oxidoreductase activity, acting on CH-OH group of donors | 3 | 1 |
GO:0016616 | oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.310 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.477 |
CLV_NRD_NRD_1 | 407 | 409 | PF00675 | 0.443 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.446 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 530 | 534 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.457 |
DEG_APCC_DBOX_1 | 224 | 232 | PF00400 | 0.529 |
DOC_CYCLIN_RxL_1 | 527 | 536 | PF00134 | 0.479 |
DOC_MAPK_DCC_7 | 77 | 87 | PF00069 | 0.468 |
DOC_MAPK_gen_1 | 113 | 122 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 37 | 44 | PF00069 | 0.474 |
DOC_MAPK_gen_1 | 406 | 413 | PF00069 | 0.396 |
DOC_MAPK_gen_1 | 542 | 550 | PF00069 | 0.433 |
DOC_MAPK_MEF2A_6 | 225 | 234 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 37 | 44 | PF00069 | 0.462 |
DOC_PP2B_LxvP_1 | 382 | 385 | PF13499 | 0.483 |
DOC_PP2B_LxvP_1 | 64 | 67 | PF13499 | 0.490 |
DOC_PP4_FxxP_1 | 133 | 136 | PF00568 | 0.448 |
DOC_PP4_FxxP_1 | 170 | 173 | PF00568 | 0.362 |
DOC_PP4_MxPP_1 | 80 | 83 | PF00568 | 0.468 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 149 | 153 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 375 | 379 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.496 |
DOC_USP7_UBL2_3 | 233 | 237 | PF12436 | 0.475 |
DOC_WW_Pin1_4 | 115 | 120 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 363 | 368 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.760 |
LIG_14-3-3_CanoR_1 | 109 | 115 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 150 | 155 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 18 | 24 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 49 | 55 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 530 | 540 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 59 | 67 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 69 | 78 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 97 | 107 | PF00244 | 0.465 |
LIG_Actin_WH2_2 | 82 | 99 | PF00022 | 0.466 |
LIG_BIR_III_4 | 278 | 282 | PF00653 | 0.475 |
LIG_BRCT_BRCA1_1 | 117 | 121 | PF00533 | 0.468 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.468 |
LIG_eIF4E_1 | 208 | 214 | PF01652 | 0.472 |
LIG_eIF4E_1 | 260 | 266 | PF01652 | 0.468 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.526 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.558 |
LIG_Integrin_RGD_1 | 183 | 185 | PF01839 | 0.275 |
LIG_LIR_Apic_2 | 167 | 173 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 227 | 236 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 26 | 35 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 500 | 509 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 227 | 232 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 26 | 30 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 500 | 505 | PF02991 | 0.575 |
LIG_MYND_1 | 94 | 98 | PF01753 | 0.435 |
LIG_PCNA_PIPBox_1 | 537 | 546 | PF02747 | 0.460 |
LIG_Pex14_2 | 133 | 137 | PF04695 | 0.450 |
LIG_SH2_CRK | 304 | 308 | PF00017 | 0.529 |
LIG_SH2_CRK | 416 | 420 | PF00017 | 0.385 |
LIG_SH2_CRK | 479 | 483 | PF00017 | 0.338 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.504 |
LIG_SH2_GRB2like | 88 | 91 | PF00017 | 0.481 |
LIG_SH2_SRC | 88 | 91 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 110 | 114 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 260 | 264 | PF00017 | 0.451 |
LIG_SH2_STAP1 | 561 | 565 | PF00017 | 0.398 |
LIG_SH2_STAT3 | 561 | 564 | PF00017 | 0.446 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 304 | 307 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 404 | 407 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 439 | 442 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.493 |
LIG_SH3_3 | 446 | 452 | PF00018 | 0.661 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.498 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.459 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.409 |
LIG_TYR_ITIM | 302 | 307 | PF00017 | 0.529 |
LIG_UBA3_1 | 249 | 255 | PF00899 | 0.460 |
LIG_UBA3_1 | 292 | 301 | PF00899 | 0.529 |
MOD_CDK_SPxxK_3 | 414 | 421 | PF00069 | 0.386 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.487 |
MOD_CK1_1 | 238 | 244 | PF00069 | 0.451 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.719 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.618 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.430 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.649 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.680 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.516 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.614 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.659 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.462 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.295 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.275 |
MOD_GlcNHglycan | 278 | 282 | PF01048 | 0.352 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.672 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.501 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.620 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.504 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.492 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.495 |
MOD_GSK3_1 | 149 | 156 | PF00069 | 0.584 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.458 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.697 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.397 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.474 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.400 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.673 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.502 |
MOD_LATS_1 | 436 | 442 | PF00433 | 0.430 |
MOD_N-GLC_1 | 359 | 364 | PF02516 | 0.550 |
MOD_N-GLC_1 | 441 | 446 | PF02516 | 0.572 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.476 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.481 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.578 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.475 |
MOD_NEK2_1 | 482 | 487 | PF00069 | 0.391 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.527 |
MOD_NEK2_2 | 340 | 345 | PF00069 | 0.570 |
MOD_PIKK_1 | 519 | 525 | PF00454 | 0.656 |
MOD_PIKK_1 | 560 | 566 | PF00454 | 0.517 |
MOD_PIKK_1 | 69 | 75 | PF00454 | 0.521 |
MOD_PKA_1 | 150 | 156 | PF00069 | 0.504 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.496 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.468 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.503 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.470 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.501 |
MOD_PKB_1 | 148 | 156 | PF00069 | 0.504 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.482 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.341 |
MOD_ProDKin_1 | 115 | 121 | PF00069 | 0.464 |
MOD_ProDKin_1 | 363 | 369 | PF00069 | 0.641 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.410 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.378 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.754 |
MOD_SUMO_for_1 | 344 | 347 | PF00179 | 0.554 |
TRG_DiLeu_BaEn_1 | 467 | 472 | PF01217 | 0.367 |
TRG_DiLeu_BaLyEn_6 | 197 | 202 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 422 | 427 | PF01217 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 428 | 433 | PF01217 | 0.418 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 416 | 419 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.506 |
TRG_ER_diArg_1 | 406 | 408 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.493 |
TRG_NES_CRM1_1 | 247 | 262 | PF08389 | 0.495 |
TRG_NLS_MonoExtC_3 | 253 | 259 | PF00514 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 254 | 259 | PF00026 | 0.285 |
TRG_Pf-PMV_PEXEL_1 | 69 | 73 | PF00026 | 0.516 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4R8 | Leptomonas seymouri | 58% | 100% |
A4HEX6 | Leishmania braziliensis | 77% | 100% |
A4I250 | Leishmania infantum | 99% | 100% |
E9AYA0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q973 | Leishmania major | 92% | 100% |