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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000417 | HIR complex | 2 | 2 |
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0005840 | ribosome | 5 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0043226 | organelle | 2 | 11 |
GO:0043228 | non-membrane-bounded organelle | 3 | 7 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:1990904 | ribonucleoprotein complex | 2 | 7 |
GO:0005634 | nucleus | 5 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 9 |
Related structures:
AlphaFold database: Q4Q1H1
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006325 | chromatin organization | 4 | 11 |
GO:0006351 | DNA-templated transcription | 7 | 11 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0009058 | biosynthetic process | 2 | 11 |
GO:0009059 | macromolecule biosynthetic process | 4 | 11 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016043 | cellular component organization | 3 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0018130 | heterocycle biosynthetic process | 4 | 11 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 11 |
GO:0032774 | RNA biosynthetic process | 5 | 11 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 11 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0044249 | cellular biosynthetic process | 3 | 11 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0071840 | cellular component organization or biogenesis | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:0097659 | nucleic acid-templated transcription | 6 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 11 |
GO:1901576 | organic substance biosynthetic process | 3 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 379 | 383 | PF00656 | 0.545 |
CLV_C14_Caspase3-7 | 80 | 84 | PF00656 | 0.506 |
CLV_NRD_NRD_1 | 277 | 279 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.294 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 614 | 616 | PF00675 | 0.765 |
CLV_NRD_NRD_1 | 638 | 640 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 641 | 643 | PF00675 | 0.616 |
CLV_PCSK_FUR_1 | 490 | 494 | PF00082 | 0.657 |
CLV_PCSK_FUR_1 | 639 | 643 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 277 | 279 | PF00082 | 0.463 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.313 |
CLV_PCSK_KEX2_1 | 492 | 494 | PF00082 | 0.588 |
CLV_PCSK_KEX2_1 | 641 | 643 | PF00082 | 0.640 |
CLV_PCSK_PC1ET2_1 | 641 | 643 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.161 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 533 | 537 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.236 |
CLV_Separin_Fungi | 596 | 602 | PF03568 | 0.536 |
DOC_MAPK_gen_1 | 589 | 597 | PF00069 | 0.584 |
DOC_MAPK_MEF2A_6 | 589 | 597 | PF00069 | 0.549 |
DOC_PP1_RVXF_1 | 241 | 248 | PF00149 | 0.302 |
DOC_PP1_RVXF_1 | 299 | 306 | PF00149 | 0.397 |
DOC_PP1_RVXF_1 | 417 | 424 | PF00149 | 0.313 |
DOC_PP2B_LxvP_1 | 312 | 315 | PF13499 | 0.387 |
DOC_PP2B_LxvP_1 | 422 | 425 | PF13499 | 0.346 |
DOC_PP4_FxxP_1 | 427 | 430 | PF00568 | 0.436 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 579 | 583 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 599 | 603 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 621 | 625 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 631 | 635 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 652 | 656 | PF00917 | 0.571 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.317 |
DOC_WW_Pin1_4 | 356 | 361 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 574 | 579 | PF00397 | 0.607 |
LIG_14-3-3_CanoR_1 | 116 | 122 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 252 | 258 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 413 | 422 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 523 | 530 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 533 | 540 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 592 | 598 | PF00244 | 0.558 |
LIG_AP2alpha_2 | 248 | 250 | PF02296 | 0.331 |
LIG_deltaCOP1_diTrp_1 | 248 | 257 | PF00928 | 0.336 |
LIG_deltaCOP1_diTrp_1 | 40 | 45 | PF00928 | 0.520 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.553 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.343 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.460 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.628 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.430 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.516 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.302 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.462 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.463 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.725 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.621 |
LIG_FHA_2 | 64 | 70 | PF00498 | 0.502 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.449 |
LIG_LIR_Gen_1 | 248 | 257 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 500 | 507 | PF02991 | 0.265 |
LIG_LIR_Gen_1 | 525 | 535 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 553 | 561 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 119 | 124 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 183 | 188 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 248 | 253 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 299 | 303 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 500 | 505 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 525 | 530 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 553 | 558 | PF02991 | 0.335 |
LIG_NRBOX | 582 | 588 | PF00104 | 0.589 |
LIG_PDZ_Class_1 | 669 | 674 | PF00595 | 0.636 |
LIG_Pex14_1 | 423 | 427 | PF04695 | 0.341 |
LIG_Pex14_2 | 253 | 257 | PF04695 | 0.425 |
LIG_SH2_CRK | 300 | 304 | PF00017 | 0.388 |
LIG_SH2_CRK | 316 | 320 | PF00017 | 0.508 |
LIG_SH2_PTP2 | 555 | 558 | PF00017 | 0.304 |
LIG_SH2_STAP1 | 199 | 203 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 548 | 552 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 291 | 294 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 501 | 504 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 516 | 519 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 548 | 551 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 573 | 576 | PF00017 | 0.631 |
LIG_SH3_2 | 30 | 35 | PF14604 | 0.456 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.515 |
LIG_SUMO_SIM_anti_2 | 38 | 43 | PF11976 | 0.383 |
LIG_SUMO_SIM_anti_2 | 633 | 639 | PF11976 | 0.678 |
LIG_SUMO_SIM_par_1 | 332 | 338 | PF11976 | 0.400 |
LIG_TYR_ITIM | 298 | 303 | PF00017 | 0.460 |
LIG_TYR_ITIM | 314 | 319 | PF00017 | 0.367 |
LIG_UBA3_1 | 333 | 342 | PF00899 | 0.587 |
LIG_WRC_WIRS_1 | 254 | 259 | PF05994 | 0.311 |
MOD_CDK_SPxxK_3 | 356 | 363 | PF00069 | 0.554 |
MOD_CDK_SPxxK_3 | 574 | 581 | PF00069 | 0.605 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.705 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.451 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.289 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.621 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.690 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.708 |
MOD_CK1_1 | 522 | 528 | PF00069 | 0.412 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.486 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.621 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.676 |
MOD_CMANNOS | 247 | 250 | PF00535 | 0.323 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.287 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.599 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.656 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.742 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.326 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.404 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.606 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.566 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.616 |
MOD_GlcNHglycan | 606 | 609 | PF01048 | 0.629 |
MOD_GlcNHglycan | 620 | 624 | PF01048 | 0.668 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.756 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.289 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.720 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.434 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.547 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.465 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.616 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.610 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.728 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.552 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.514 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.400 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.479 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.614 |
MOD_LATS_1 | 531 | 537 | PF00433 | 0.374 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.355 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.417 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.191 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.436 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.381 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.360 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.346 |
MOD_NEK2_1 | 561 | 566 | PF00069 | 0.482 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.496 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.556 |
MOD_PIKK_1 | 438 | 444 | PF00454 | 0.607 |
MOD_PIKK_1 | 478 | 484 | PF00454 | 0.578 |
MOD_PKA_2 | 522 | 528 | PF00069 | 0.393 |
MOD_PKA_2 | 600 | 606 | PF00069 | 0.620 |
MOD_Plk_1 | 343 | 349 | PF00069 | 0.518 |
MOD_Plk_1 | 542 | 548 | PF00069 | 0.402 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.498 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.319 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.391 |
MOD_Plk_4 | 652 | 658 | PF00069 | 0.548 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.286 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.316 |
MOD_ProDKin_1 | 356 | 362 | PF00069 | 0.733 |
MOD_ProDKin_1 | 574 | 580 | PF00069 | 0.603 |
MOD_SUMO_for_1 | 270 | 273 | PF00179 | 0.591 |
MOD_SUMO_rev_2 | 137 | 144 | PF00179 | 0.289 |
MOD_SUMO_rev_2 | 178 | 187 | PF00179 | 0.546 |
TRG_DiLeu_BaEn_1 | 50 | 55 | PF01217 | 0.580 |
TRG_DiLeu_BaEn_4 | 50 | 56 | PF01217 | 0.494 |
TRG_ENDOCYTIC_2 | 188 | 191 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 316 | 319 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.352 |
TRG_ER_diArg_1 | 277 | 279 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 300 | 302 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 34 | 37 | PF00400 | 0.395 |
TRG_ER_diArg_1 | 490 | 493 | PF00400 | 0.674 |
TRG_NLS_MonoCore_2 | 638 | 643 | PF00514 | 0.561 |
TRG_NLS_MonoExtC_3 | 638 | 643 | PF00514 | 0.561 |
TRG_NLS_MonoExtN_4 | 639 | 644 | PF00514 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 413 | 417 | PF00026 | 0.315 |
TRG_Pf-PMV_PEXEL_1 | 533 | 537 | PF00026 | 0.340 |
TRG_PTS2 | 1 | 45 | PF00400 | 0.544 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBV3 | Leptomonas seymouri | 63% | 99% |
A0A1X0P8Z1 | Trypanosomatidae | 45% | 100% |
A0A3S7XAX4 | Leishmania donovani | 90% | 100% |
A0A422NCI3 | Trypanosoma rangeli | 47% | 100% |
A4HPB6 | Leishmania braziliensis | 81% | 100% |
A4ICF6 | Leishmania infantum | 90% | 100% |
D0A3C6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AT27 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BH36 | Trypanosoma cruzi | 47% | 100% |