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:0005840 | ribosome | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HKP1
Term | Name | Level | Count |
---|---|---|---|
GO:0006412 | translation | 4 | 2 |
GO:0006518 | peptide metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 2 |
GO:0043043 | peptide biosynthetic process | 5 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043603 | amide metabolic process | 3 | 2 |
GO:0043604 | amide biosynthetic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003735 | structural constituent of ribosome | 2 | 2 |
GO:0005198 | structural molecule activity | 1 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 273 | 277 | PF00656 | 0.620 |
CLV_C14_Caspase3-7 | 388 | 392 | PF00656 | 0.454 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.501 |
CLV_PCSK_FUR_1 | 303 | 307 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.716 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 255 | 257 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 268 | 270 | PF00082 | 0.639 |
CLV_PCSK_PC1ET2_1 | 304 | 306 | PF00082 | 0.336 |
CLV_PCSK_PC7_1 | 134 | 140 | PF00082 | 0.552 |
CLV_PCSK_PC7_1 | 345 | 351 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 453 | 457 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 512 | 516 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 619 | 623 | PF00082 | 0.570 |
DEG_APCC_DBOX_1 | 114 | 122 | PF00400 | 0.558 |
DEG_APCC_DBOX_1 | 642 | 650 | PF00400 | 0.363 |
DEG_ODPH_VHL_1 | 476 | 487 | PF01847 | 0.483 |
DEG_SPOP_SBC_1 | 489 | 493 | PF00917 | 0.496 |
DEG_SPOP_SBC_1 | 624 | 628 | PF00917 | 0.325 |
DEG_SPOP_SBC_1 | 636 | 640 | PF00917 | 0.438 |
DOC_CYCLIN_RxL_1 | 120 | 132 | PF00134 | 0.504 |
DOC_MAPK_DCC_7 | 224 | 234 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 120 | 129 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 427 | 436 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 123 | 131 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 174 | 183 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 427 | 436 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 516 | 523 | PF00069 | 0.271 |
DOC_MAPK_MEF2A_6 | 573 | 582 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 643 | 652 | PF00069 | 0.416 |
DOC_PP1_RVXF_1 | 518 | 524 | PF00149 | 0.406 |
DOC_PP2B_LxvP_1 | 456 | 459 | PF13499 | 0.617 |
DOC_PP4_FxxP_1 | 663 | 666 | PF00568 | 0.358 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.770 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.774 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.607 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 632 | 637 | PF00397 | 0.570 |
LIG_14-3-3_CanoR_1 | 149 | 155 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 619 | 624 | PF00244 | 0.496 |
LIG_Actin_WH2_2 | 364 | 381 | PF00022 | 0.388 |
LIG_BIR_III_4 | 164 | 168 | PF00653 | 0.475 |
LIG_deltaCOP1_diTrp_1 | 435 | 441 | PF00928 | 0.251 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.646 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.581 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.446 |
LIG_FHA_1 | 471 | 477 | PF00498 | 0.669 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.481 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.581 |
LIG_FHA_1 | 603 | 609 | PF00498 | 0.439 |
LIG_FHA_1 | 616 | 622 | PF00498 | 0.515 |
LIG_FHA_1 | 625 | 631 | PF00498 | 0.446 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.541 |
LIG_FHA_2 | 564 | 570 | PF00498 | 0.566 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.704 |
LIG_IRF3_LxIS_1 | 578 | 583 | PF10401 | 0.281 |
LIG_LIR_Gen_1 | 435 | 445 | PF02991 | 0.265 |
LIG_LIR_Gen_1 | 503 | 509 | PF02991 | 0.532 |
LIG_LIR_LC3C_4 | 627 | 632 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 503 | 507 | PF02991 | 0.543 |
LIG_NRBOX | 563 | 569 | PF00104 | 0.351 |
LIG_PCNA_PIPBox_1 | 649 | 658 | PF02747 | 0.272 |
LIG_RPA_C_Fungi | 144 | 156 | PF08784 | 0.472 |
LIG_SH2_GRB2like | 294 | 297 | PF00017 | 0.328 |
LIG_SH2_PTP2 | 328 | 331 | PF00017 | 0.513 |
LIG_SH2_STAT3 | 39 | 42 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 310 | 313 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.513 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.264 |
LIG_SH3_3 | 320 | 326 | PF00018 | 0.496 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.627 |
LIG_SH3_3 | 482 | 488 | PF00018 | 0.490 |
LIG_SH3_3 | 618 | 624 | PF00018 | 0.509 |
LIG_SH3_3 | 642 | 648 | PF00018 | 0.391 |
LIG_SUMO_SIM_par_1 | 604 | 609 | PF11976 | 0.402 |
LIG_TRAF2_1 | 332 | 335 | PF00917 | 0.468 |
LIG_TRAF2_1 | 553 | 556 | PF00917 | 0.294 |
LIG_TYR_ITIM | 292 | 297 | PF00017 | 0.349 |
LIG_WRC_WIRS_1 | 382 | 387 | PF05994 | 0.396 |
LIG_WRC_WIRS_1 | 544 | 549 | PF05994 | 0.358 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.436 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.584 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.511 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.664 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.605 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.673 |
MOD_CK1_1 | 557 | 563 | PF00069 | 0.557 |
MOD_CK1_1 | 626 | 632 | PF00069 | 0.469 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.601 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.587 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.600 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.589 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.440 |
MOD_CK2_1 | 550 | 556 | PF00069 | 0.281 |
MOD_CK2_1 | 563 | 569 | PF00069 | 0.558 |
MOD_CK2_1 | 580 | 586 | PF00069 | 0.476 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.509 |
MOD_Cter_Amidation | 266 | 269 | PF01082 | 0.649 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.567 |
MOD_GlcNHglycan | 151 | 154 | PF01048 | 0.444 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.497 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.566 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.447 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.299 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.495 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.348 |
MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.504 |
MOD_GlcNHglycan | 632 | 635 | PF01048 | 0.685 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.557 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.578 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.645 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.692 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.573 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.604 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.453 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.534 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.635 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.390 |
MOD_GSK3_1 | 576 | 583 | PF00069 | 0.404 |
MOD_GSK3_1 | 611 | 618 | PF00069 | 0.478 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.410 |
MOD_GSK3_1 | 632 | 639 | PF00069 | 0.547 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.595 |
MOD_N-GLC_2 | 225 | 227 | PF02516 | 0.446 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.612 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.369 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.542 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.348 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.483 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.547 |
MOD_NEK2_1 | 440 | 445 | PF00069 | 0.457 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.546 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.458 |
MOD_NEK2_1 | 580 | 585 | PF00069 | 0.449 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.507 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.563 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.505 |
MOD_NEK2_2 | 21 | 26 | PF00069 | 0.401 |
MOD_NEK2_2 | 481 | 486 | PF00069 | 0.487 |
MOD_PIKK_1 | 297 | 303 | PF00454 | 0.470 |
MOD_PIKK_1 | 385 | 391 | PF00454 | 0.519 |
MOD_PIKK_1 | 546 | 552 | PF00454 | 0.331 |
MOD_PIKK_1 | 573 | 579 | PF00454 | 0.337 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.617 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.595 |
MOD_PKA_2 | 611 | 617 | PF00069 | 0.471 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.514 |
MOD_PKB_1 | 137 | 145 | PF00069 | 0.508 |
MOD_Plk_1 | 145 | 151 | PF00069 | 0.585 |
MOD_Plk_1 | 420 | 426 | PF00069 | 0.312 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.517 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.520 |
MOD_Plk_4 | 554 | 560 | PF00069 | 0.444 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.434 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.391 |
MOD_Plk_4 | 626 | 632 | PF00069 | 0.582 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.492 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.432 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.613 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.429 |
MOD_ProDKin_1 | 632 | 638 | PF00069 | 0.572 |
MOD_SUMO_for_1 | 70 | 73 | PF00179 | 0.626 |
TRG_DiLeu_BaEn_2 | 341 | 347 | PF01217 | 0.369 |
TRG_DiLeu_BaLyEn_6 | 228 | 233 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.488 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 183 | 185 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 254 | 257 | PF00400 | 0.536 |
TRG_ER_diArg_1 | 303 | 306 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 348 | 350 | PF00400 | 0.312 |
TRG_ER_diArg_1 | 426 | 429 | PF00400 | 0.561 |
TRG_NLS_MonoCore_2 | 302 | 307 | PF00514 | 0.334 |
TRG_NLS_MonoExtN_4 | 303 | 308 | PF00514 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 34 | 38 | PF00026 | 0.497 |
TRG_Pf-PMV_PEXEL_1 | 552 | 556 | PF00026 | 0.299 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5A1 | Leptomonas seymouri | 45% | 100% |
A0A1X0NRK2 | Trypanosomatidae | 30% | 100% |
A0A3Q8IG27 | Leishmania donovani | 73% | 100% |
A4I872 | Leishmania infantum | 73% | 100% |
D0AAE1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9B330 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4Q524 | Leishmania major | 72% | 100% |
V5AUP9 | Trypanosoma cruzi | 31% | 100% |