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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005829 | cytosol | 2 | 1 |
GO:0030684 | preribosome | 3 | 1 |
GO:0030688 | preribosome, small subunit precursor | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HHE8
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 8 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 8 |
GO:0042274 | ribosomal small subunit biogenesis | 5 | 8 |
GO:0044085 | cellular component biogenesis | 3 | 8 |
GO:0071840 | cellular component organization or biogenesis | 2 | 8 |
GO:0000054 | ribosomal subunit export from nucleus | 3 | 1 |
GO:0000056 | ribosomal small subunit export from nucleus | 4 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006913 | nucleocytoplasmic transport | 5 | 1 |
GO:0031503 | protein-containing complex localization | 2 | 1 |
GO:0033750 | ribosome localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051168 | nuclear export | 6 | 1 |
GO:0051169 | nuclear transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051640 | organelle localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051656 | establishment of organelle localization | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.625 |
CLV_C14_Caspase3-7 | 69 | 73 | PF00656 | 0.500 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 230 | 232 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 563 | 565 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 575 | 577 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 586 | 588 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.510 |
CLV_PCSK_FUR_1 | 228 | 232 | PF00082 | 0.622 |
CLV_PCSK_FUR_1 | 584 | 588 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 373 | 375 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 484 | 486 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 563 | 565 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.433 |
CLV_PCSK_KEX2_1 | 586 | 588 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 606 | 608 | PF00082 | 0.331 |
CLV_PCSK_KEX2_1 | 615 | 617 | PF00082 | 0.502 |
CLV_PCSK_PC7_1 | 224 | 230 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 587 | 591 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 607 | 611 | PF00082 | 0.328 |
DEG_SCF_TRCP1_1 | 540 | 546 | PF00400 | 0.535 |
DEG_SPOP_SBC_1 | 390 | 394 | PF00917 | 0.519 |
DEG_SPOP_SBC_1 | 508 | 512 | PF00917 | 0.630 |
DOC_PP1_RVXF_1 | 614 | 621 | PF00149 | 0.583 |
DOC_PP2B_LxvP_1 | 400 | 403 | PF13499 | 0.519 |
DOC_PP4_FxxP_1 | 123 | 126 | PF00568 | 0.522 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 390 | 394 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 489 | 493 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 508 | 512 | PF00917 | 0.663 |
DOC_USP7_UBL2_3 | 526 | 530 | PF12436 | 0.643 |
DOC_USP7_UBL2_3 | 565 | 569 | PF12436 | 0.534 |
DOC_USP7_UBL2_3 | 590 | 594 | PF12436 | 0.464 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.534 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.764 |
LIG_14-3-3_CanoR_1 | 41 | 49 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 453 | 461 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 587 | 597 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 606 | 613 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 615 | 619 | PF00244 | 0.564 |
LIG_BIR_III_4 | 23 | 27 | PF00653 | 0.636 |
LIG_BIR_III_4 | 344 | 348 | PF00653 | 0.599 |
LIG_Clathr_ClatBox_1 | 418 | 422 | PF01394 | 0.633 |
LIG_deltaCOP1_diTrp_1 | 191 | 196 | PF00928 | 0.496 |
LIG_deltaCOP1_diTrp_1 | 89 | 99 | PF00928 | 0.688 |
LIG_EVH1_1 | 400 | 404 | PF00568 | 0.516 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.517 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.526 |
LIG_FHA_1 | 453 | 459 | PF00498 | 0.472 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.437 |
LIG_FHA_1 | 7 | 13 | PF00498 | 0.478 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.514 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.623 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.679 |
LIG_FHA_2 | 566 | 572 | PF00498 | 0.469 |
LIG_FHA_2 | 594 | 600 | PF00498 | 0.534 |
LIG_LIR_Apic_2 | 120 | 126 | PF02991 | 0.521 |
LIG_LIR_Apic_2 | 440 | 446 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 265 | 275 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 13 | 17 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 194 | 199 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 204 | 210 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 265 | 271 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 437 | 442 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 596 | 600 | PF02991 | 0.518 |
LIG_Pex14_2 | 361 | 365 | PF04695 | 0.458 |
LIG_RPA_C_Fungi | 219 | 231 | PF08784 | 0.576 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.512 |
LIG_SH2_CRK | 443 | 447 | PF00017 | 0.535 |
LIG_SH2_GRB2like | 442 | 445 | PF00017 | 0.472 |
LIG_SH2_NCK_1 | 443 | 447 | PF00017 | 0.535 |
LIG_SH2_NCK_1 | 62 | 66 | PF00017 | 0.586 |
LIG_SH2_STAP1 | 439 | 443 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 62 | 66 | PF00017 | 0.586 |
LIG_SH2_STAP1 | 83 | 87 | PF00017 | 0.572 |
LIG_SH2_STAT3 | 442 | 445 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.445 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.611 |
LIG_SH3_4 | 6 | 13 | PF00018 | 0.532 |
LIG_SUMO_SIM_anti_2 | 416 | 422 | PF11976 | 0.597 |
LIG_TRAF2_1 | 211 | 214 | PF00917 | 0.405 |
LIG_TRAF2_1 | 303 | 306 | PF00917 | 0.448 |
LIG_TRAF2_1 | 404 | 407 | PF00917 | 0.682 |
LIG_TRAF2_1 | 411 | 414 | PF00917 | 0.648 |
LIG_TRAF2_1 | 568 | 571 | PF00917 | 0.477 |
LIG_TRAF2_1 | 77 | 80 | PF00917 | 0.654 |
LIG_TRFH_1 | 14 | 18 | PF08558 | 0.512 |
LIG_TYR_ITIM | 12 | 17 | PF00017 | 0.504 |
LIG_UBA3_1 | 327 | 332 | PF00899 | 0.546 |
LIG_UBA3_1 | 418 | 426 | PF00899 | 0.606 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.558 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.469 |
MOD_CK1_1 | 492 | 498 | PF00069 | 0.737 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.666 |
MOD_CK1_1 | 608 | 614 | PF00069 | 0.522 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.522 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.541 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.530 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.513 |
MOD_CK2_1 | 464 | 470 | PF00069 | 0.720 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.693 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.536 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.691 |
MOD_CK2_1 | 565 | 571 | PF00069 | 0.475 |
MOD_CK2_1 | 593 | 599 | PF00069 | 0.536 |
MOD_CMANNOS | 193 | 196 | PF00535 | 0.500 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.630 |
MOD_GlcNHglycan | 148 | 152 | PF01048 | 0.556 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.565 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.432 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.492 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.762 |
MOD_GlcNHglycan | 491 | 494 | PF01048 | 0.742 |
MOD_GlcNHglycan | 511 | 514 | PF01048 | 0.695 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.663 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.648 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.799 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.525 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.516 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.634 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.616 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.562 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.642 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.476 |
MOD_GSK3_1 | 488 | 495 | PF00069 | 0.650 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.716 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.652 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.638 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.716 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.482 |
MOD_LATS_1 | 533 | 539 | PF00433 | 0.540 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.672 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.474 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.568 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.519 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.436 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.538 |
MOD_NEK2_1 | 605 | 610 | PF00069 | 0.415 |
MOD_NEK2_2 | 614 | 619 | PF00069 | 0.507 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.544 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.534 |
MOD_PIKK_1 | 608 | 614 | PF00454 | 0.522 |
MOD_PKA_1 | 223 | 229 | PF00069 | 0.576 |
MOD_PKA_1 | 526 | 532 | PF00069 | 0.605 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.576 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.587 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.574 |
MOD_PKA_2 | 605 | 611 | PF00069 | 0.571 |
MOD_PKA_2 | 614 | 620 | PF00069 | 0.523 |
MOD_PKB_1 | 229 | 237 | PF00069 | 0.467 |
MOD_Plk_1 | 395 | 401 | PF00069 | 0.525 |
MOD_Plk_1 | 570 | 576 | PF00069 | 0.474 |
MOD_Plk_2-3 | 283 | 289 | PF00069 | 0.517 |
MOD_Plk_2-3 | 540 | 546 | PF00069 | 0.535 |
MOD_Plk_2-3 | 599 | 605 | PF00069 | 0.530 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.525 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.472 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.744 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.677 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.775 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.765 |
MOD_SUMO_rev_2 | 154 | 163 | PF00179 | 0.607 |
MOD_SUMO_rev_2 | 416 | 425 | PF00179 | 0.609 |
MOD_SUMO_rev_2 | 539 | 549 | PF00179 | 0.566 |
MOD_SUMO_rev_2 | 566 | 574 | PF00179 | 0.476 |
MOD_SUMO_rev_2 | 98 | 108 | PF00179 | 0.693 |
TRG_DiLeu_BaEn_1 | 205 | 210 | PF01217 | 0.536 |
TRG_DiLeu_BaEn_1 | 414 | 419 | PF01217 | 0.633 |
TRG_DiLeu_LyEn_5 | 205 | 210 | PF01217 | 0.536 |
TRG_ENDOCYTIC_2 | 14 | 17 | PF00928 | 0.527 |
TRG_ENDOCYTIC_2 | 597 | 600 | PF00928 | 0.455 |
TRG_ER_diArg_1 | 222 | 224 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 228 | 231 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 372 | 374 | PF00400 | 0.530 |
TRG_ER_diArg_1 | 377 | 380 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 484 | 486 | PF00400 | 0.529 |
TRG_ER_diArg_1 | 562 | 564 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 574 | 576 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 605 | 607 | PF00400 | 0.544 |
TRG_NLS_MonoCore_2 | 4 | 9 | PF00514 | 0.531 |
TRG_NLS_MonoExtC_3 | 458 | 463 | PF00514 | 0.474 |
TRG_NLS_MonoExtN_4 | 2 | 9 | PF00514 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 208 | 212 | PF00026 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 262 | 267 | PF00026 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 535 | 540 | PF00026 | 0.543 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2D0 | Leptomonas seymouri | 48% | 88% |
A0A3Q8IHA2 | Leishmania donovani | 67% | 96% |
A4I4J8 | Leishmania infantum | 67% | 96% |
E9ADZ7 | Leishmania major | 67% | 100% |
E9ALT4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 67% | 94% |
V5BH77 | Trypanosoma cruzi | 38% | 100% |