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: A0A3Q8ICM1
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0016491 | oxidoreductase activity | 2 | 10 |
GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 10 |
GO:0017150 | tRNA dihydrouridine synthase activity | 5 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0050660 | flavin adenine dinucleotide binding | 4 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0106413 | dihydrouridine synthase activity | 4 | 10 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 10 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 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 | 555 | 559 | PF00656 | 0.427 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.246 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.263 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.763 |
CLV_PCSK_KEX2_1 | 296 | 298 | PF00082 | 0.246 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.702 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.278 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.763 |
CLV_PCSK_PC1ET2_1 | 345 | 347 | PF00082 | 0.510 |
CLV_PCSK_PC7_1 | 84 | 90 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 22 | 26 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 424 | 428 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.506 |
DEG_APCC_DBOX_1 | 532 | 540 | PF00400 | 0.529 |
DOC_ANK_TNKS_1 | 623 | 630 | PF00023 | 0.511 |
DOC_CYCLIN_yCln2_LP_2 | 322 | 328 | PF00134 | 0.463 |
DOC_MAPK_gen_1 | 547 | 556 | PF00069 | 0.564 |
DOC_MAPK_gen_1 | 641 | 649 | PF00069 | 0.614 |
DOC_MAPK_MEF2A_6 | 505 | 513 | PF00069 | 0.447 |
DOC_PP2B_LxvP_1 | 322 | 325 | PF13499 | 0.463 |
DOC_PP4_FxxP_1 | 333 | 336 | PF00568 | 0.529 |
DOC_PP4_FxxP_1 | 470 | 473 | PF00568 | 0.463 |
DOC_SPAK_OSR1_1 | 232 | 236 | PF12202 | 0.392 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.519 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 568 | 572 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.615 |
DOC_USP7_UBL2_3 | 639 | 643 | PF12436 | 0.641 |
DOC_WW_Pin1_4 | 139 | 144 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.712 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.536 |
LIG_14-3-3_CanoR_1 | 22 | 27 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 490 | 498 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 623 | 628 | PF00244 | 0.566 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.501 |
LIG_BIR_III_4 | 425 | 429 | PF00653 | 0.471 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.529 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.487 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.534 |
LIG_FHA_1 | 325 | 331 | PF00498 | 0.529 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.529 |
LIG_FHA_1 | 494 | 500 | PF00498 | 0.587 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.496 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.549 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.462 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.462 |
LIG_FHA_2 | 544 | 550 | PF00498 | 0.694 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.449 |
LIG_GBD_Chelix_1 | 314 | 322 | PF00786 | 0.340 |
LIG_Integrin_isoDGR_2 | 30 | 32 | PF01839 | 0.516 |
LIG_LIR_Gen_1 | 158 | 166 | PF02991 | 0.592 |
LIG_LIR_Gen_1 | 306 | 315 | PF02991 | 0.446 |
LIG_LIR_Gen_1 | 383 | 393 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 441 | 449 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 125 | 131 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 158 | 163 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 306 | 311 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 441 | 445 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 9 | 14 | PF02991 | 0.452 |
LIG_PDZ_Class_2 | 655 | 660 | PF00595 | 0.659 |
LIG_Pex14_1 | 503 | 507 | PF04695 | 0.529 |
LIG_Pex14_2 | 519 | 523 | PF04695 | 0.488 |
LIG_SH2_CRK | 11 | 15 | PF00017 | 0.470 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.498 |
LIG_SH2_NCK_1 | 61 | 65 | PF00017 | 0.454 |
LIG_SH2_SRC | 442 | 445 | PF00017 | 0.529 |
LIG_SH2_STAP1 | 386 | 390 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 442 | 446 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.459 |
LIG_SH3_2 | 476 | 481 | PF14604 | 0.529 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.488 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.500 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.698 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.482 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.575 |
LIG_SUMO_SIM_anti_2 | 379 | 386 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 614 | 620 | PF11976 | 0.378 |
LIG_SUMO_SIM_par_1 | 645 | 652 | PF11976 | 0.647 |
LIG_TRAF2_1 | 165 | 168 | PF00917 | 0.502 |
LIG_TRAF2_1 | 356 | 359 | PF00917 | 0.520 |
LIG_TRAF2_1 | 642 | 645 | PF00917 | 0.631 |
LIG_WRC_WIRS_1 | 300 | 305 | PF05994 | 0.463 |
MOD_CDK_SPxxK_3 | 63 | 70 | PF00069 | 0.454 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.631 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.498 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.691 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.554 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.501 |
MOD_CK2_1 | 528 | 534 | PF00069 | 0.471 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.609 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.537 |
MOD_CMANNOS | 50 | 53 | PF00535 | 0.367 |
MOD_Cter_Amidation | 30 | 33 | PF01082 | 0.508 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.495 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.556 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.483 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.612 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.329 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.271 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.634 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.698 |
MOD_GlcNHglycan | 583 | 589 | PF01048 | 0.647 |
MOD_GlcNHglycan | 599 | 602 | PF01048 | 0.599 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.750 |
MOD_GlcNHglycan | 79 | 83 | PF01048 | 0.741 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.456 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.516 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.612 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.529 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.511 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.631 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.522 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.470 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.761 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.525 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.517 |
MOD_N-GLC_1 | 350 | 355 | PF02516 | 0.464 |
MOD_NEK2_1 | 106 | 111 | PF00069 | 0.521 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.498 |
MOD_NEK2_1 | 310 | 315 | PF00069 | 0.518 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.462 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.446 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.553 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.532 |
MOD_NEK2_2 | 189 | 194 | PF00069 | 0.610 |
MOD_PIKK_1 | 471 | 477 | PF00454 | 0.498 |
MOD_PK_1 | 623 | 629 | PF00069 | 0.472 |
MOD_PKA_1 | 623 | 629 | PF00069 | 0.472 |
MOD_PKA_1 | 88 | 94 | PF00069 | 0.499 |
MOD_PKA_2 | 489 | 495 | PF00069 | 0.520 |
MOD_PKA_2 | 623 | 629 | PF00069 | 0.535 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.555 |
MOD_Plk_1 | 173 | 179 | PF00069 | 0.454 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.575 |
MOD_Plk_1 | 569 | 575 | PF00069 | 0.580 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.590 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.317 |
MOD_Plk_4 | 299 | 305 | PF00069 | 0.455 |
MOD_Plk_4 | 310 | 316 | PF00069 | 0.431 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.479 |
MOD_ProDKin_1 | 139 | 145 | PF00069 | 0.446 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.718 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.530 |
MOD_SUMO_for_1 | 642 | 645 | PF00179 | 0.631 |
MOD_SUMO_rev_2 | 162 | 172 | PF00179 | 0.542 |
MOD_SUMO_rev_2 | 461 | 470 | PF00179 | 0.529 |
TRG_DiLeu_BaEn_1 | 306 | 311 | PF01217 | 0.451 |
TRG_DiLeu_BaEn_4 | 534 | 540 | PF01217 | 0.498 |
TRG_DiLeu_BaEn_4 | 651 | 657 | PF01217 | 0.537 |
TRG_DiLeu_BaLyEn_6 | 459 | 464 | PF01217 | 0.463 |
TRG_ENDOCYTIC_2 | 11 | 14 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 386 | 389 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.505 |
TRG_ER_diArg_1 | 420 | 422 | PF00400 | 0.463 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.585 |
TRG_NES_CRM1_1 | 309 | 323 | PF08389 | 0.456 |
TRG_Pf-PMV_PEXEL_1 | 12 | 17 | PF00026 | 0.569 |
TRG_Pf-PMV_PEXEL_1 | 129 | 134 | PF00026 | 0.329 |
TRG_Pf-PMV_PEXEL_1 | 388 | 392 | PF00026 | 0.318 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HS31 | Leptomonas seymouri | 61% | 100% |
A0A0S4JUA9 | Bodo saltans | 38% | 100% |
A4HJH5 | Leishmania braziliensis | 79% | 100% |
A4I6W8 | Leishmania infantum | 100% | 100% |
C9ZWQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B1Z2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q669 | Leishmania major | 92% | 100% |
V5D2B4 | Trypanosoma cruzi | 41% | 100% |