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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: E9B3R5
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0008670 | 2,4-dienoyl-CoA reductase (NADPH) activity | 5 | 6 |
GO:0010181 | FMN binding | 4 | 10 |
GO:0016491 | oxidoreductase activity | 2 | 10 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 6 |
GO:0016628 | oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor | 4 | 6 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:1901265 | nucleoside phosphate binding | 3 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.484 |
CLV_C14_Caspase3-7 | 559 | 563 | PF00656 | 0.376 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 521 | 523 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.325 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 435 | 437 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.287 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.207 |
CLV_PCSK_PC1ET2_1 | 435 | 437 | PF00082 | 0.353 |
CLV_PCSK_PC7_1 | 290 | 296 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 605 | 609 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 613 | 617 | PF00082 | 0.243 |
CLV_PCSK_SKI1_1 | 693 | 697 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.247 |
DEG_APCC_DBOX_1 | 205 | 213 | PF00400 | 0.421 |
DEG_APCC_DBOX_1 | 227 | 235 | PF00400 | 0.504 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.502 |
DEG_SPOP_SBC_1 | 542 | 546 | PF00917 | 0.374 |
DEG_SPOP_SBC_1 | 584 | 588 | PF00917 | 0.237 |
DOC_ANK_TNKS_1 | 521 | 528 | PF00023 | 0.353 |
DOC_CKS1_1 | 606 | 611 | PF01111 | 0.285 |
DOC_CYCLIN_yCln2_LP_2 | 31 | 37 | PF00134 | 0.475 |
DOC_CYCLIN_yCln2_LP_2 | 333 | 339 | PF00134 | 0.463 |
DOC_CYCLIN_yCln2_LP_2 | 603 | 609 | PF00134 | 0.334 |
DOC_MAPK_DCC_7 | 295 | 305 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 204 | 211 | PF00069 | 0.421 |
DOC_MAPK_gen_1 | 294 | 302 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 455 | 462 | PF00069 | 0.273 |
DOC_MAPK_gen_1 | 59 | 68 | PF00069 | 0.439 |
DOC_MAPK_gen_1 | 667 | 676 | PF00069 | 0.384 |
DOC_MAPK_gen_1 | 712 | 720 | PF00069 | 0.448 |
DOC_MAPK_HePTP_8 | 137 | 149 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 140 | 149 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 294 | 302 | PF00069 | 0.426 |
DOC_MAPK_MEF2A_6 | 455 | 464 | PF00069 | 0.403 |
DOC_MAPK_MEF2A_6 | 6 | 15 | PF00069 | 0.282 |
DOC_PP1_RVXF_1 | 202 | 208 | PF00149 | 0.463 |
DOC_PP2B_LxvP_1 | 387 | 390 | PF13499 | 0.398 |
DOC_PP2B_PxIxI_1 | 300 | 306 | PF00149 | 0.504 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 412 | 416 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 542 | 546 | PF00917 | 0.157 |
DOC_USP7_MATH_1 | 584 | 588 | PF00917 | 0.312 |
DOC_USP7_MATH_1 | 590 | 594 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.314 |
DOC_USP7_UBL2_3 | 2 | 6 | PF12436 | 0.441 |
DOC_USP7_UBL2_3 | 569 | 573 | PF12436 | 0.367 |
DOC_USP7_UBL2_3 | 689 | 693 | PF12436 | 0.273 |
DOC_USP7_UBL2_3 | 713 | 717 | PF12436 | 0.453 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.429 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.466 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.322 |
DOC_WW_Pin1_4 | 594 | 599 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 605 | 610 | PF00397 | 0.194 |
DOC_WW_Pin1_4 | 693 | 698 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.438 |
LIG_14-3-3_CanoR_1 | 228 | 232 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 279 | 285 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 330 | 336 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 467 | 471 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 645 | 650 | PF00244 | 0.418 |
LIG_Actin_WH2_2 | 198 | 215 | PF00022 | 0.463 |
LIG_BIR_III_4 | 217 | 221 | PF00653 | 0.475 |
LIG_Clathr_ClatBox_1 | 662 | 666 | PF01394 | 0.285 |
LIG_CtBP_PxDLS_1 | 10 | 14 | PF00389 | 0.438 |
LIG_CtBP_PxDLS_1 | 142 | 146 | PF00389 | 0.504 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.502 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.509 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.326 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.339 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.451 |
LIG_FHA_1 | 631 | 637 | PF00498 | 0.270 |
LIG_FHA_1 | 658 | 664 | PF00498 | 0.285 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.381 |
LIG_FHA_1 | 681 | 687 | PF00498 | 0.389 |
LIG_FHA_1 | 694 | 700 | PF00498 | 0.481 |
LIG_FHA_1 | 709 | 715 | PF00498 | 0.551 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.447 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.432 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.438 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.438 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.293 |
LIG_FHA_2 | 417 | 423 | PF00498 | 0.222 |
LIG_FHA_2 | 467 | 473 | PF00498 | 0.306 |
LIG_FHA_2 | 483 | 489 | PF00498 | 0.344 |
LIG_FHA_2 | 554 | 560 | PF00498 | 0.427 |
LIG_IBAR_NPY_1 | 47 | 49 | PF08397 | 0.504 |
LIG_LIR_Gen_1 | 12 | 23 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 155 | 164 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 501 | 506 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 653 | 657 | PF02991 | 0.282 |
LIG_LRP6_Inhibitor_1 | 641 | 647 | PF00058 | 0.152 |
LIG_LYPXL_yS_3 | 503 | 506 | PF13949 | 0.285 |
LIG_OCRL_FandH_1 | 184 | 196 | PF00620 | 0.441 |
LIG_PDZ_Class_2 | 725 | 730 | PF00595 | 0.305 |
LIG_Pex14_2 | 223 | 227 | PF04695 | 0.438 |
LIG_Pex14_2 | 566 | 570 | PF04695 | 0.258 |
LIG_PTB_Apo_2 | 685 | 692 | PF02174 | 0.396 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.376 |
LIG_SH2_CRK | 49 | 53 | PF00017 | 0.504 |
LIG_SH2_SRC | 478 | 481 | PF00017 | 0.317 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.319 |
LIG_SH2_STAP1 | 478 | 482 | PF00017 | 0.317 |
LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 509 | 513 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.258 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 664 | 667 | PF00017 | 0.317 |
LIG_SH3_3 | 603 | 609 | PF00018 | 0.334 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.480 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.450 |
LIG_SUMO_SIM_anti_2 | 170 | 178 | PF11976 | 0.421 |
LIG_SUMO_SIM_anti_2 | 230 | 237 | PF11976 | 0.424 |
LIG_SUMO_SIM_par_1 | 671 | 678 | PF11976 | 0.334 |
LIG_TRAF2_1 | 469 | 472 | PF00917 | 0.285 |
LIG_TRAF2_1 | 578 | 581 | PF00917 | 0.227 |
LIG_UBA3_1 | 496 | 502 | PF00899 | 0.353 |
LIG_WW_1 | 609 | 612 | PF00397 | 0.152 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.325 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.282 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.290 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.374 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.283 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.282 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.258 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.285 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.318 |
MOD_CK2_1 | 505 | 511 | PF00069 | 0.440 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.427 |
MOD_CK2_1 | 684 | 690 | PF00069 | 0.334 |
MOD_Cter_Amidation | 519 | 522 | PF01082 | 0.299 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.338 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.354 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.179 |
MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.377 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.358 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.322 |
MOD_GlcNHglycan | 492 | 495 | PF01048 | 0.349 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.401 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.334 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.409 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.273 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.347 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.244 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.380 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.374 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.292 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.381 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.407 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.328 |
MOD_GSK3_1 | 584 | 591 | PF00069 | 0.432 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.282 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.374 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.490 |
MOD_N-GLC_1 | 423 | 428 | PF02516 | 0.242 |
MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.369 |
MOD_N-GLC_1 | 708 | 713 | PF02516 | 0.465 |
MOD_N-GLC_2 | 351 | 353 | PF02516 | 0.281 |
MOD_N-GLC_2 | 594 | 596 | PF02516 | 0.285 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.356 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.282 |
MOD_NEK2_1 | 618 | 623 | PF00069 | 0.329 |
MOD_NEK2_1 | 629 | 634 | PF00069 | 0.293 |
MOD_NEK2_1 | 657 | 662 | PF00069 | 0.285 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.282 |
MOD_NEK2_2 | 450 | 455 | PF00069 | 0.380 |
MOD_NEK2_2 | 458 | 463 | PF00069 | 0.353 |
MOD_PIKK_1 | 130 | 136 | PF00454 | 0.323 |
MOD_PIKK_1 | 237 | 243 | PF00454 | 0.317 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.363 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.258 |
MOD_PKA_2 | 466 | 472 | PF00069 | 0.373 |
MOD_Plk_1 | 143 | 149 | PF00069 | 0.342 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.256 |
MOD_Plk_1 | 458 | 464 | PF00069 | 0.354 |
MOD_Plk_1 | 613 | 619 | PF00069 | 0.317 |
MOD_Plk_1 | 670 | 676 | PF00069 | 0.334 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.282 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.258 |
MOD_Plk_4 | 613 | 619 | PF00069 | 0.289 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.290 |
MOD_ProDKin_1 | 117 | 123 | PF00069 | 0.269 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.321 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.374 |
MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.322 |
MOD_ProDKin_1 | 594 | 600 | PF00069 | 0.408 |
MOD_ProDKin_1 | 605 | 611 | PF00069 | 0.194 |
MOD_ProDKin_1 | 693 | 699 | PF00069 | 0.522 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.282 |
MOD_SUMO_rev_2 | 580 | 584 | PF00179 | 0.321 |
TRG_DiLeu_BaEn_3 | 104 | 110 | PF01217 | 0.204 |
TRG_DiLeu_BaLyEn_6 | 145 | 150 | PF01217 | 0.365 |
TRG_DiLeu_BaLyEn_6 | 298 | 303 | PF01217 | 0.374 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 612 | 615 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 654 | 657 | PF00928 | 0.258 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.282 |
TRG_ER_diArg_1 | 204 | 207 | PF00400 | 0.258 |
TRG_ER_diArg_1 | 293 | 295 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 521 | 523 | PF00400 | 0.287 |
TRG_ER_diArg_1 | 566 | 568 | PF00400 | 0.152 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P302 | Leptomonas seymouri | 72% | 100% |
A0A0N0P5L6 | Leptomonas seymouri | 32% | 100% |
A0A0S4JCH5 | Bodo saltans | 29% | 100% |
A0A0S4JST7 | Bodo saltans | 46% | 100% |
A0A1X0NKW1 | Trypanosomatidae | 29% | 100% |
A0A1X0NU55 | Trypanosomatidae | 53% | 100% |
A0A3S5H5T4 | Leishmania donovani | 31% | 100% |
A0A3S7X6G9 | Leishmania donovani | 95% | 100% |
A4H4Q6 | Leishmania braziliensis | 31% | 100% |
A4HLD7 | Leishmania braziliensis | 85% | 100% |
A4HSY5 | Leishmania infantum | 31% | 100% |
A4I8U6 | Leishmania infantum | 94% | 100% |
A4J778 | Desulforamulus reducens (strain ATCC BAA-1160 / DSM 100696 / MI-1) | 32% | 100% |
C9ZTL4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AKX1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 100% |
G9F1Y9 | Clostridium sporogenes (strain ATCC 7955 / DSM 767 / NBRC 16411 / NCIMB 8053 / NCTC 8594 / PA 3679) | 30% | 100% |
O87278 | Rhizobium meliloti (strain 1021) | 31% | 100% |
P16099 | Methylophilus methylotrophus | 27% | 100% |
P19410 | Clostridium scindens (strain JCM 10418 / VPI 12708) | 30% | 100% |
P32370 | Clostridium scindens (strain JCM 10418 / VPI 12708) | 29% | 100% |
P32382 | Thermoanaerobacter brockii | 34% | 100% |
P42593 | Escherichia coli (strain K12) | 44% | 100% |
Q48303 | Hyphomicrobium sp. (strain x) | 26% | 99% |
Q4Q4A9 | Leishmania major | 93% | 100% |
Q4QIY4 | Leishmania major | 32% | 100% |
V5AR23 | Trypanosoma cruzi | 52% | 100% |
V5BNI9 | Trypanosoma cruzi | 31% | 100% |