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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 9 |
GO:0043226 | organelle | 2 | 9 |
GO:0043227 | membrane-bounded organelle | 3 | 9 |
GO:0043229 | intracellular organelle | 3 | 9 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4HLZ3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006351 | DNA-templated transcription | 7 | 3 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009058 | biosynthetic process | 2 | 3 |
GO:0009059 | macromolecule biosynthetic process | 4 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016070 | RNA metabolic process | 5 | 3 |
GO:0018130 | heterocycle biosynthetic process | 4 | 3 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 3 |
GO:0032774 | RNA biosynthetic process | 5 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0044249 | cellular biosynthetic process | 3 | 3 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 3 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0090304 | nucleic acid metabolic process | 4 | 3 |
GO:0097659 | nucleic acid-templated transcription | 6 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 3 |
GO:1901576 | organic substance biosynthetic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0008270 | zinc ion binding | 6 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043169 | cation binding | 3 | 2 |
GO:0046872 | metal ion binding | 4 | 2 |
GO:0046914 | transition metal ion binding | 5 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 102 | 106 | PF00656 | 0.434 |
CLV_C14_Caspase3-7 | 394 | 398 | PF00656 | 0.586 |
CLV_C14_Caspase3-7 | 420 | 424 | PF00656 | 0.400 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.645 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 278 | 280 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.301 |
CLV_NRD_NRD_1 | 468 | 470 | PF00675 | 0.373 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.486 |
CLV_PCSK_FUR_1 | 200 | 204 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 160 | 162 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.603 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 285 | 287 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 468 | 470 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 493 | 495 | PF00082 | 0.481 |
CLV_PCSK_PC1ET2_1 | 160 | 162 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 171 | 173 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.443 |
DEG_SCF_FBW7_1 | 113 | 120 | PF00400 | 0.695 |
DOC_CKS1_1 | 114 | 119 | PF01111 | 0.619 |
DOC_CYCLIN_RxL_1 | 465 | 473 | PF00134 | 0.414 |
DOC_MAPK_DCC_7 | 494 | 504 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 326 | 335 | PF00069 | 0.540 |
DOC_MAPK_HePTP_8 | 492 | 504 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 326 | 335 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 352 | 361 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 495 | 504 | PF00069 | 0.449 |
DOC_PP4_FxxP_1 | 354 | 357 | PF00568 | 0.513 |
DOC_PP4_FxxP_1 | 534 | 537 | PF00568 | 0.655 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 556 | 560 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 99 | 103 | PF00917 | 0.546 |
DOC_USP7_UBL2_3 | 160 | 164 | PF12436 | 0.601 |
DOC_USP7_UBL2_3 | 166 | 170 | PF12436 | 0.597 |
DOC_WW_Pin1_4 | 113 | 118 | PF00397 | 0.732 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 505 | 510 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 516 | 521 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.529 |
LIG_14-3-3_CanoR_1 | 285 | 293 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 352 | 357 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 540 | 549 | PF00244 | 0.542 |
LIG_Actin_WH2_2 | 314 | 331 | PF00022 | 0.505 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.678 |
LIG_BIR_III_2 | 105 | 109 | PF00653 | 0.647 |
LIG_BRCT_BRCA1_1 | 530 | 534 | PF00533 | 0.688 |
LIG_CSL_BTD_1 | 23 | 26 | PF09270 | 0.448 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.457 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.415 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.516 |
LIG_FHA_1 | 540 | 546 | PF00498 | 0.547 |
LIG_FHA_1 | 579 | 585 | PF00498 | 0.439 |
LIG_FHA_2 | 217 | 223 | PF00498 | 0.600 |
LIG_FHA_2 | 262 | 268 | PF00498 | 0.668 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.532 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.457 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.393 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.584 |
LIG_FHA_2 | 415 | 421 | PF00498 | 0.431 |
LIG_FHA_2 | 434 | 440 | PF00498 | 0.416 |
LIG_FHA_2 | 508 | 514 | PF00498 | 0.628 |
LIG_GSK3_LRP6_1 | 113 | 119 | PF00069 | 0.542 |
LIG_LIR_Apic_2 | 353 | 357 | PF02991 | 0.393 |
LIG_LIR_Apic_2 | 531 | 537 | PF02991 | 0.620 |
LIG_LIR_Apic_2 | 543 | 549 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 13 | 22 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 136 | 144 | PF02991 | 0.689 |
LIG_LIR_Gen_1 | 228 | 238 | PF02991 | 0.503 |
LIG_LIR_Nem_3 | 13 | 17 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 136 | 142 | PF02991 | 0.691 |
LIG_LIR_Nem_3 | 228 | 234 | PF02991 | 0.509 |
LIG_NRBOX | 466 | 472 | PF00104 | 0.424 |
LIG_PALB2_WD40_1 | 365 | 373 | PF16756 | 0.448 |
LIG_PTB_Apo_2 | 364 | 371 | PF02174 | 0.516 |
LIG_SH2_CRK | 278 | 282 | PF00017 | 0.586 |
LIG_SH2_CRK | 546 | 550 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 561 | 565 | PF00017 | 0.506 |
LIG_SH2_STAT3 | 249 | 252 | PF00017 | 0.602 |
LIG_SH2_STAT3 | 561 | 564 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 477 | 480 | PF00017 | 0.560 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.663 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.527 |
LIG_SH3_3 | 20 | 26 | PF00018 | 0.462 |
LIG_SH3_3 | 517 | 523 | PF00018 | 0.612 |
LIG_SUMO_SIM_anti_2 | 41 | 49 | PF11976 | 0.520 |
LIG_SUMO_SIM_anti_2 | 427 | 432 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 450 | 455 | PF11976 | 0.398 |
LIG_TRAF2_1 | 108 | 111 | PF00917 | 0.650 |
LIG_TRAF2_1 | 209 | 212 | PF00917 | 0.597 |
LIG_TRAF2_1 | 417 | 420 | PF00917 | 0.403 |
LIG_TRAF2_1 | 93 | 96 | PF00917 | 0.473 |
LIG_TRFH_1 | 258 | 262 | PF08558 | 0.614 |
LIG_UBA3_1 | 321 | 329 | PF00899 | 0.348 |
LIG_WRC_WIRS_1 | 351 | 356 | PF05994 | 0.419 |
MOD_CDK_SPK_2 | 266 | 271 | PF00069 | 0.620 |
MOD_CDK_SPxxK_3 | 533 | 540 | PF00069 | 0.613 |
MOD_CK1_1 | 120 | 126 | PF00069 | 0.667 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.561 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.557 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.402 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.556 |
MOD_CK1_1 | 424 | 430 | PF00069 | 0.531 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.593 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.646 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.689 |
MOD_CK1_1 | 559 | 565 | PF00069 | 0.653 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.495 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.711 |
MOD_CK2_1 | 250 | 256 | PF00069 | 0.577 |
MOD_CK2_1 | 286 | 292 | PF00069 | 0.505 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.320 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.423 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.648 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.631 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.777 |
MOD_GlcNHglycan | 221 | 226 | PF01048 | 0.723 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.547 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.611 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.540 |
MOD_GlcNHglycan | 308 | 311 | PF01048 | 0.579 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.563 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.402 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.552 |
MOD_GlcNHglycan | 525 | 530 | PF01048 | 0.536 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.317 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.318 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.673 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.593 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.768 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.537 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.635 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.448 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.406 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.387 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.448 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.627 |
MOD_GSK3_1 | 512 | 519 | PF00069 | 0.758 |
MOD_GSK3_1 | 540 | 547 | PF00069 | 0.458 |
MOD_N-GLC_1 | 331 | 336 | PF02516 | 0.193 |
MOD_N-GLC_1 | 421 | 426 | PF02516 | 0.402 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.582 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.508 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.508 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.466 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.418 |
MOD_OFUCOSY | 390 | 395 | PF10250 | 0.576 |
MOD_PIKK_1 | 294 | 300 | PF00454 | 0.458 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.393 |
MOD_PIKK_1 | 333 | 339 | PF00454 | 0.414 |
MOD_PIKK_1 | 508 | 514 | PF00454 | 0.601 |
MOD_PKA_1 | 202 | 208 | PF00069 | 0.535 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.670 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.753 |
MOD_PKA_2 | 250 | 256 | PF00069 | 0.594 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.457 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.570 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.526 |
MOD_PKB_1 | 200 | 208 | PF00069 | 0.534 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.549 |
MOD_Plk_1 | 331 | 337 | PF00069 | 0.481 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.507 |
MOD_Plk_1 | 578 | 584 | PF00069 | 0.327 |
MOD_Plk_2-3 | 206 | 212 | PF00069 | 0.607 |
MOD_Plk_2-3 | 388 | 394 | PF00069 | 0.601 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.292 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.321 |
MOD_Plk_4 | 53 | 59 | PF00069 | 0.596 |
MOD_ProDKin_1 | 113 | 119 | PF00069 | 0.733 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.643 |
MOD_ProDKin_1 | 505 | 511 | PF00069 | 0.637 |
MOD_ProDKin_1 | 516 | 522 | PF00069 | 0.617 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.574 |
MOD_SUMO_for_1 | 247 | 250 | PF00179 | 0.596 |
TRG_DiLeu_BaEn_1 | 76 | 81 | PF01217 | 0.448 |
TRG_DiLeu_BaEn_2 | 298 | 304 | PF01217 | 0.454 |
TRG_DiLeu_BaLyEn_6 | 466 | 471 | PF01217 | 0.426 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.630 |
TRG_ER_diArg_1 | 200 | 203 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 467 | 469 | PF00400 | 0.393 |
TRG_ER_diArg_1 | 492 | 495 | PF00400 | 0.480 |
TRG_NLS_Bipartite_1 | 160 | 175 | PF00514 | 0.625 |
TRG_NLS_MonoCore_2 | 168 | 173 | PF00514 | 0.574 |
TRG_NLS_MonoExtC_3 | 169 | 174 | PF00514 | 0.587 |
TRG_NLS_MonoExtC_3 | 244 | 250 | PF00514 | 0.617 |
TRG_NLS_MonoExtN_4 | 166 | 173 | PF00514 | 0.683 |
TRG_Pf-PMV_PEXEL_1 | 468 | 473 | PF00026 | 0.371 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5Y6 | Leptomonas seymouri | 49% | 100% |
A0A1X0NRB1 | Trypanosomatidae | 31% | 100% |
A0A3Q8IKG6 | Leishmania donovani | 78% | 99% |
A0A422NKE1 | Trypanosoma rangeli | 31% | 100% |
A4I9C3 | Leishmania infantum | 78% | 99% |
E9B4C2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 99% |
Q4Q3Q3 | Leishmania major | 78% | 100% |