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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 18 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
Related structures:
AlphaFold database: Q4QIY4
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 18 |
GO:0003824 | catalytic activity | 1 | 18 |
GO:0005488 | binding | 1 | 18 |
GO:0010181 | FMN binding | 4 | 18 |
GO:0016491 | oxidoreductase activity | 2 | 18 |
GO:0032553 | ribonucleotide binding | 3 | 18 |
GO:0036094 | small molecule binding | 2 | 18 |
GO:0043167 | ion binding | 2 | 18 |
GO:0043168 | anion binding | 3 | 18 |
GO:0097159 | organic cyclic compound binding | 2 | 18 |
GO:0097367 | carbohydrate derivative binding | 2 | 18 |
GO:1901265 | nucleoside phosphate binding | 3 | 18 |
GO:1901363 | heterocyclic compound binding | 2 | 18 |
GO:0008670 | 2,4-dienoyl-CoA reductase (NADPH) activity | 5 | 5 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 5 |
GO:0016628 | oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor | 4 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 204 | 208 | PF00656 | 0.567 |
CLV_C14_Caspase3-7 | 701 | 705 | PF00656 | 0.362 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.278 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 650 | 652 | PF00675 | 0.278 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 215 | 217 | PF00082 | 0.281 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.286 |
CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.278 |
CLV_PCSK_PC1ET2_1 | 450 | 452 | PF00082 | 0.422 |
CLV_PCSK_PC7_1 | 129 | 135 | PF00082 | 0.222 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 346 | 350 | PF00082 | 0.256 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 651 | 655 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.293 |
DEG_APCC_DBOX_1 | 241 | 249 | PF00400 | 0.514 |
DEG_APCC_DBOX_1 | 304 | 312 | PF00400 | 0.445 |
DEG_APCC_KENBOX_2 | 454 | 458 | PF00400 | 0.459 |
DEG_SCF_FBW7_2 | 250 | 257 | PF00400 | 0.462 |
DOC_CKS1_1 | 22 | 27 | PF01111 | 0.457 |
DOC_CYCLIN_RxL_1 | 343 | 351 | PF00134 | 0.434 |
DOC_CYCLIN_yCln2_LP_2 | 22 | 28 | PF00134 | 0.435 |
DOC_MAPK_gen_1 | 215 | 223 | PF00069 | 0.494 |
DOC_MAPK_gen_1 | 402 | 412 | PF00069 | 0.321 |
DOC_MAPK_gen_1 | 428 | 435 | PF00069 | 0.278 |
DOC_MAPK_gen_1 | 467 | 476 | PF00069 | 0.342 |
DOC_MAPK_gen_1 | 560 | 569 | PF00069 | 0.259 |
DOC_MAPK_gen_1 | 588 | 598 | PF00069 | 0.264 |
DOC_MAPK_gen_1 | 89 | 97 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 215 | 223 | PF00069 | 0.456 |
DOC_MAPK_MEF2A_6 | 470 | 478 | PF00069 | 0.335 |
DOC_MAPK_MEF2A_6 | 560 | 569 | PF00069 | 0.259 |
DOC_PP2B_LxvP_1 | 521 | 524 | PF13499 | 0.303 |
DOC_PP2B_LxvP_1 | 587 | 590 | PF13499 | 0.292 |
DOC_PP4_FxxP_1 | 653 | 656 | PF00568 | 0.342 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 360 | 364 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.315 |
DOC_USP7_UBL2_3 | 332 | 336 | PF12436 | 0.502 |
DOC_USP7_UBL2_3 | 681 | 685 | PF12436 | 0.400 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.450 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.270 |
DOC_WW_Pin1_4 | 250 | 255 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.448 |
DOC_WW_Pin1_4 | 581 | 586 | PF00397 | 0.425 |
LIG_14-3-3_CanoR_1 | 134 | 143 | PF00244 | 0.440 |
LIG_14-3-3_CanoR_1 | 150 | 154 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 384 | 392 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 407 | 411 | PF00244 | 0.248 |
LIG_14-3-3_CanoR_1 | 470 | 478 | PF00244 | 0.321 |
LIG_14-3-3_CanoR_1 | 506 | 513 | PF00244 | 0.296 |
LIG_Actin_WH2_2 | 234 | 251 | PF00022 | 0.435 |
LIG_APCC_ABBA_1 | 565 | 570 | PF00400 | 0.259 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.507 |
LIG_BIR_III_4 | 207 | 211 | PF00653 | 0.422 |
LIG_BIR_III_4 | 637 | 641 | PF00653 | 0.390 |
LIG_BRCT_BRCA1_1 | 19 | 23 | PF00533 | 0.363 |
LIG_BRCT_BRCA1_1 | 649 | 653 | PF00533 | 0.254 |
LIG_FHA_1 | 108 | 114 | PF00498 | 0.445 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.478 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.432 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.450 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.308 |
LIG_FHA_1 | 419 | 425 | PF00498 | 0.301 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.298 |
LIG_FHA_1 | 613 | 619 | PF00498 | 0.271 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.422 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.478 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.279 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.322 |
LIG_HOMEOBOX | 677 | 680 | PF00046 | 0.376 |
LIG_LIR_Apic_2 | 152 | 158 | PF02991 | 0.523 |
LIG_LIR_Apic_2 | 650 | 656 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 167 | 176 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 456 | 464 | PF02991 | 0.250 |
LIG_LIR_Gen_1 | 674 | 684 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 167 | 172 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 20 | 26 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 456 | 461 | PF02991 | 0.201 |
LIG_LIR_Nem_3 | 693 | 697 | PF02991 | 0.349 |
LIG_PCNA_PIPBox_1 | 59 | 68 | PF02747 | 0.435 |
LIG_PCNA_yPIPBox_3 | 373 | 384 | PF02747 | 0.326 |
LIG_PDZ_Class_2 | 725 | 730 | PF00595 | 0.337 |
LIG_PTB_Apo_2 | 33 | 40 | PF02174 | 0.515 |
LIG_PTB_Apo_2 | 666 | 673 | PF02174 | 0.422 |
LIG_PTB_Phospho_1 | 33 | 39 | PF10480 | 0.515 |
LIG_PTB_Phospho_1 | 666 | 672 | PF10480 | 0.390 |
LIG_REV1ctd_RIR_1 | 63 | 73 | PF16727 | 0.478 |
LIG_SH2_CRK | 155 | 159 | PF00017 | 0.422 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.422 |
LIG_SH2_CRK | 458 | 462 | PF00017 | 0.198 |
LIG_SH2_GRB2like | 44 | 47 | PF00017 | 0.422 |
LIG_SH2_SRC | 291 | 294 | PF00017 | 0.515 |
LIG_SH2_SRC | 724 | 727 | PF00017 | 0.335 |
LIG_SH2_STAP1 | 169 | 173 | PF00017 | 0.478 |
LIG_SH2_STAT3 | 380 | 383 | PF00017 | 0.356 |
LIG_SH2_STAT3 | 395 | 398 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 697 | 700 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 706 | 709 | PF00017 | 0.531 |
LIG_SH3_2 | 145 | 150 | PF14604 | 0.470 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.470 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.515 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.515 |
LIG_SUMO_SIM_anti_2 | 409 | 414 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 325 | 331 | PF11976 | 0.400 |
LIG_TRAF2_1 | 483 | 486 | PF00917 | 0.382 |
LIG_WRC_WIRS_1 | 551 | 556 | PF05994 | 0.390 |
LIG_WRC_WIRS_1 | 97 | 102 | PF05994 | 0.515 |
MOD_CDK_SPxK_1 | 21 | 27 | PF00069 | 0.390 |
MOD_CDK_SPxxK_3 | 581 | 588 | PF00069 | 0.259 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.437 |
MOD_CK1_1 | 138 | 144 | PF00069 | 0.423 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.511 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.561 |
MOD_CK1_1 | 4 | 10 | PF00069 | 0.502 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.410 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.453 |
MOD_CK2_1 | 390 | 396 | PF00069 | 0.329 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.287 |
MOD_CK2_1 | 480 | 486 | PF00069 | 0.352 |
MOD_Cter_Amidation | 535 | 538 | PF01082 | 0.290 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.608 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.294 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.278 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.272 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.340 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.270 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.504 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.428 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.381 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.517 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.499 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.451 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.440 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.506 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.322 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.433 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.433 |
MOD_GSK3_1 | 698 | 705 | PF00069 | 0.367 |
MOD_N-GLC_1 | 274 | 279 | PF02516 | 0.274 |
MOD_N-GLC_1 | 668 | 673 | PF02516 | 0.259 |
MOD_N-GLC_2 | 373 | 375 | PF02516 | 0.309 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.528 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.456 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.328 |
MOD_NEK2_1 | 255 | 260 | PF00069 | 0.514 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.415 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.441 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.458 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.261 |
MOD_NEK2_1 | 529 | 534 | PF00069 | 0.259 |
MOD_NEK2_2 | 692 | 697 | PF00069 | 0.507 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.400 |
MOD_PIKK_1 | 612 | 618 | PF00454 | 0.226 |
MOD_PK_1 | 470 | 476 | PF00069 | 0.390 |
MOD_PKA_1 | 506 | 512 | PF00069 | 0.259 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.455 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.566 |
MOD_PKA_2 | 306 | 312 | PF00069 | 0.452 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.296 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.390 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.290 |
MOD_PKA_2 | 506 | 512 | PF00069 | 0.262 |
MOD_PKA_2 | 559 | 565 | PF00069 | 0.279 |
MOD_PKA_2 | 702 | 708 | PF00069 | 0.459 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.515 |
MOD_Plk_1 | 274 | 280 | PF00069 | 0.507 |
MOD_Plk_1 | 363 | 369 | PF00069 | 0.538 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.247 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.259 |
MOD_Plk_1 | 668 | 674 | PF00069 | 0.290 |
MOD_Plk_1 | 692 | 698 | PF00069 | 0.396 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.407 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.529 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.284 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.290 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.272 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.228 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.397 |
MOD_Plk_4 | 594 | 600 | PF00069 | 0.359 |
MOD_Plk_4 | 623 | 629 | PF00069 | 0.261 |
MOD_Plk_4 | 656 | 662 | PF00069 | 0.317 |
MOD_Plk_4 | 671 | 677 | PF00069 | 0.351 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.450 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.270 |
MOD_ProDKin_1 | 250 | 256 | PF00069 | 0.462 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.448 |
MOD_ProDKin_1 | 581 | 587 | PF00069 | 0.425 |
TRG_DiLeu_BaEn_1 | 577 | 582 | PF01217 | 0.390 |
TRG_DiLeu_BaLyEn_6 | 344 | 349 | PF01217 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 517 | 522 | PF01217 | 0.371 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.422 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 677 | 680 | PF00928 | 0.397 |
TRG_ER_diArg_1 | 132 | 135 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 427 | 429 | PF00400 | 0.278 |
TRG_ER_diArg_1 | 505 | 507 | PF00400 | 0.259 |
TRG_ER_diArg_1 | 537 | 539 | PF00400 | 0.286 |
TRG_NLS_MonoExtN_4 | 129 | 136 | PF00514 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 346 | 351 | PF00026 | 0.237 |
TRG_Pf-PMV_PEXEL_1 | 467 | 471 | PF00026 | 0.303 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P302 | Leptomonas seymouri | 31% | 100% |
A0A0N0P5L6 | Leptomonas seymouri | 84% | 100% |
A0A0S4JCH5 | Bodo saltans | 55% | 100% |
A0A0S4JST7 | Bodo saltans | 32% | 100% |
A0A1X0NKW1 | Trypanosomatidae | 68% | 100% |
A0A1X0NU55 | Trypanosomatidae | 32% | 100% |
A0A3S5H5T4 | Leishmania donovani | 97% | 100% |
A0A3S7X6G9 | Leishmania donovani | 32% | 100% |
A4H4Q6 | Leishmania braziliensis | 92% | 99% |
A4HLD7 | Leishmania braziliensis | 31% | 100% |
A4HSY5 | Leishmania infantum | 97% | 100% |
A4I8U6 | Leishmania infantum | 32% | 100% |
A4J778 | Desulforamulus reducens (strain ATCC BAA-1160 / DSM 100696 / MI-1) | 28% | 100% |
C9ZTL4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 69% | 100% |
E9AKX1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
E9B3R5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
G9F1Y9 | Clostridium sporogenes (strain ATCC 7955 / DSM 767 / NBRC 16411 / NCIMB 8053 / NCTC 8594 / PA 3679) | 27% | 100% |
P16099 | Methylophilus methylotrophus | 25% | 100% |
P19410 | Clostridium scindens (strain JCM 10418 / VPI 12708) | 28% | 100% |
P32370 | Clostridium scindens (strain JCM 10418 / VPI 12708) | 28% | 100% |
P32382 | Thermoanaerobacter brockii | 28% | 100% |
P42593 | Escherichia coli (strain K12) | 31% | 100% |
Q48303 | Hyphomicrobium sp. (strain x) | 26% | 99% |
Q4Q4A9 | Leishmania major | 32% | 100% |
V5AR23 | Trypanosoma cruzi | 32% | 100% |
V5BNI9 | Trypanosoma cruzi | 70% | 100% |