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:0005634 | nucleus | 5 | 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 |
Related structures:
AlphaFold database: A4HKZ2
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 10 |
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004386 | helicase activity | 2 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0005524 | ATP binding | 5 | 10 |
GO:0017076 | purine nucleotide binding | 4 | 10 |
GO:0030554 | adenyl nucleotide binding | 5 | 10 |
GO:0032553 | ribonucleotide binding | 3 | 10 |
GO:0032555 | purine ribonucleotide binding | 4 | 10 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 10 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 10 |
GO:0036094 | small molecule binding | 2 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043168 | anion binding | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0097367 | carbohydrate derivative binding | 2 | 10 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 10 |
GO:0140657 | ATP-dependent activity | 1 | 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 | 420 | 424 | PF00656 | 0.760 |
CLV_C14_Caspase3-7 | 475 | 479 | PF00656 | 0.503 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.356 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 537 | 539 | PF00675 | 0.701 |
CLV_NRD_NRD_1 | 587 | 589 | PF00675 | 0.503 |
CLV_NRD_NRD_1 | 664 | 666 | PF00675 | 0.471 |
CLV_PCSK_FUR_1 | 499 | 503 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 14 | 16 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.347 |
CLV_PCSK_KEX2_1 | 267 | 269 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.615 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 587 | 589 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.501 |
CLV_PCSK_PC1ET2_1 | 14 | 16 | PF00082 | 0.634 |
CLV_PCSK_PC1ET2_1 | 259 | 261 | PF00082 | 0.349 |
CLV_PCSK_PC1ET2_1 | 267 | 269 | PF00082 | 0.312 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 43 | 45 | PF00082 | 0.683 |
CLV_PCSK_PC7_1 | 256 | 262 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.290 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 345 | 349 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.714 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 643 | 647 | PF00082 | 0.548 |
CLV_Separin_Metazoa | 225 | 229 | PF03568 | 0.531 |
DEG_APCC_DBOX_1 | 399 | 407 | PF00400 | 0.528 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.717 |
DEG_SIAH_1 | 75 | 83 | PF03145 | 0.628 |
DEG_SPOP_SBC_1 | 117 | 121 | PF00917 | 0.716 |
DEG_SPOP_SBC_1 | 577 | 581 | PF00917 | 0.474 |
DOC_CKS1_1 | 248 | 253 | PF01111 | 0.474 |
DOC_CKS1_1 | 39 | 44 | PF01111 | 0.478 |
DOC_CYCLIN_RxL_1 | 311 | 320 | PF00134 | 0.591 |
DOC_CYCLIN_RxL_1 | 344 | 356 | PF00134 | 0.624 |
DOC_CYCLIN_RxL_1 | 9 | 22 | PF00134 | 0.700 |
DOC_MAPK_gen_1 | 164 | 173 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 318 | 328 | PF00069 | 0.502 |
DOC_MAPK_gen_1 | 499 | 508 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 630 | 640 | PF00069 | 0.456 |
DOC_MAPK_gen_1 | 664 | 671 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 9 | 18 | PF00069 | 0.723 |
DOC_MAPK_HePTP_8 | 8 | 20 | PF00069 | 0.650 |
DOC_MAPK_MEF2A_6 | 11 | 20 | PF00069 | 0.743 |
DOC_MAPK_MEF2A_6 | 153 | 161 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 321 | 330 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 633 | 640 | PF00069 | 0.498 |
DOC_PP1_RVXF_1 | 202 | 208 | PF00149 | 0.490 |
DOC_PP1_RVXF_1 | 34 | 41 | PF00149 | 0.637 |
DOC_PP2B_LxvP_1 | 601 | 604 | PF13499 | 0.472 |
DOC_PP2B_PxIxI_1 | 243 | 249 | PF00149 | 0.527 |
DOC_PP4_FxxP_1 | 446 | 449 | PF00568 | 0.271 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.779 |
DOC_USP7_MATH_1 | 572 | 576 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 577 | 581 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 634 | 638 | PF00917 | 0.519 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 564 | 569 | PF00397 | 0.739 |
LIG_14-3-3_CanoR_1 | 172 | 180 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 19 | 24 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 53 | 59 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 588 | 598 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 633 | 639 | PF00244 | 0.564 |
LIG_Actin_WH2_2 | 16 | 33 | PF00022 | 0.646 |
LIG_BRCT_BRCA1_1 | 119 | 123 | PF00533 | 0.663 |
LIG_CaM_IQ_9 | 392 | 407 | PF13499 | 0.573 |
LIG_Clathr_ClatBox_1 | 290 | 294 | PF01394 | 0.490 |
LIG_deltaCOP1_diTrp_1 | 190 | 198 | PF00928 | 0.537 |
LIG_deltaCOP1_diTrp_1 | 252 | 257 | PF00928 | 0.508 |
LIG_eIF4E_1 | 346 | 352 | PF01652 | 0.601 |
LIG_FHA_1 | 152 | 158 | PF00498 | 0.444 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.530 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.490 |
LIG_FHA_1 | 221 | 227 | PF00498 | 0.490 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.497 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.403 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.503 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.540 |
LIG_FHA_1 | 490 | 496 | PF00498 | 0.554 |
LIG_FHA_1 | 605 | 611 | PF00498 | 0.428 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.416 |
LIG_FHA_1 | 87 | 93 | PF00498 | 0.334 |
LIG_FHA_2 | 247 | 253 | PF00498 | 0.591 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.437 |
LIG_FHA_2 | 615 | 621 | PF00498 | 0.554 |
LIG_GBD_Chelix_1 | 485 | 493 | PF00786 | 0.377 |
LIG_HCF-1_HBM_1 | 216 | 219 | PF13415 | 0.561 |
LIG_LIR_Apic_2 | 195 | 200 | PF02991 | 0.561 |
LIG_LIR_Apic_2 | 320 | 325 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 25 | 33 | PF02991 | 0.594 |
LIG_LIR_Gen_1 | 278 | 285 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 442 | 449 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 25 | 30 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 442 | 446 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 534 | 539 | PF02991 | 0.653 |
LIG_MYND_1 | 412 | 416 | PF01753 | 0.707 |
LIG_PCNA_PIPBox_1 | 130 | 139 | PF02747 | 0.411 |
LIG_PCNA_yPIPBox_3 | 304 | 317 | PF02747 | 0.499 |
LIG_PTB_Apo_2 | 239 | 246 | PF02174 | 0.561 |
LIG_PTB_Phospho_1 | 239 | 245 | PF10480 | 0.561 |
LIG_RPA_C_Fungi | 256 | 268 | PF08784 | 0.401 |
LIG_RPA_C_Fungi | 359 | 371 | PF08784 | 0.637 |
LIG_SH2_CRK | 219 | 223 | PF00017 | 0.344 |
LIG_SH2_CRK | 322 | 326 | PF00017 | 0.358 |
LIG_SH2_PTP2 | 245 | 248 | PF00017 | 0.321 |
LIG_SH2_SRC | 94 | 97 | PF00017 | 0.584 |
LIG_SH2_STAP1 | 277 | 281 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 491 | 495 | PF00017 | 0.449 |
LIG_SH2_STAT3 | 138 | 141 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 391 | 394 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 443 | 446 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 525 | 528 | PF00017 | 0.470 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.452 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.444 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.321 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.485 |
LIG_SH3_3 | 458 | 464 | PF00018 | 0.505 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.502 |
LIG_SUMO_SIM_anti_2 | 175 | 181 | PF11976 | 0.444 |
LIG_SUMO_SIM_anti_2 | 286 | 292 | PF11976 | 0.343 |
LIG_SUMO_SIM_anti_2 | 607 | 613 | PF11976 | 0.422 |
LIG_SUMO_SIM_anti_2 | 637 | 642 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 175 | 181 | PF11976 | 0.444 |
LIG_SUMO_SIM_par_1 | 289 | 295 | PF11976 | 0.344 |
LIG_SUMO_SIM_par_1 | 75 | 81 | PF11976 | 0.414 |
LIG_TRAF2_1 | 395 | 398 | PF00917 | 0.463 |
LIG_TRFH_1 | 279 | 283 | PF08558 | 0.369 |
LIG_UBA3_1 | 133 | 140 | PF00899 | 0.233 |
LIG_UBA3_1 | 312 | 321 | PF00899 | 0.344 |
MOD_CDK_SPK_2 | 38 | 43 | PF00069 | 0.487 |
MOD_CDK_SPxK_1 | 38 | 44 | PF00069 | 0.486 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.678 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.659 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.730 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.718 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.542 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.419 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.473 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.450 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.529 |
MOD_CK2_1 | 614 | 620 | PF00069 | 0.448 |
MOD_GlcNHglycan | 305 | 308 | PF01048 | 0.467 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.344 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.731 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.628 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.613 |
MOD_GlcNHglycan | 542 | 546 | PF01048 | 0.593 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.698 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.713 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.426 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.757 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.427 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.588 |
MOD_GSK3_1 | 299 | 306 | PF00069 | 0.467 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.344 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.588 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.376 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.793 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.486 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.665 |
MOD_GSK3_1 | 589 | 596 | PF00069 | 0.364 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.567 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.622 |
MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.444 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.444 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.401 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.375 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.384 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.416 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.482 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.715 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.575 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.545 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.449 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.459 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.583 |
MOD_NEK2_2 | 589 | 594 | PF00069 | 0.413 |
MOD_PIKK_1 | 392 | 398 | PF00454 | 0.572 |
MOD_PIKK_1 | 472 | 478 | PF00454 | 0.709 |
MOD_PIKK_1 | 553 | 559 | PF00454 | 0.791 |
MOD_PIKK_1 | 86 | 92 | PF00454 | 0.527 |
MOD_PK_1 | 19 | 25 | PF00069 | 0.692 |
MOD_PKA_1 | 220 | 226 | PF00069 | 0.369 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.344 |
MOD_PKA_2 | 303 | 309 | PF00069 | 0.463 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.434 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.631 |
MOD_PKA_2 | 52 | 58 | PF00069 | 0.556 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.611 |
MOD_PKB_1 | 500 | 508 | PF00069 | 0.612 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.615 |
MOD_Plk_1 | 489 | 495 | PF00069 | 0.607 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.561 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.401 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.595 |
MOD_Plk_4 | 636 | 642 | PF00069 | 0.441 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.344 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.482 |
MOD_ProDKin_1 | 564 | 570 | PF00069 | 0.740 |
TRG_DiLeu_BaEn_2 | 503 | 509 | PF01217 | 0.610 |
TRG_DiLeu_BaEn_4 | 25 | 31 | PF01217 | 0.729 |
TRG_DiLeu_BaLyEn_6 | 169 | 174 | PF01217 | 0.233 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 245 | 248 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.529 |
TRG_ER_diArg_1 | 2 | 5 | PF00400 | 0.605 |
TRG_ER_diArg_1 | 219 | 221 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 260 | 262 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.470 |
TRG_ER_diArg_1 | 499 | 502 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 536 | 538 | PF00400 | 0.694 |
TRG_NES_CRM1_1 | 483 | 498 | PF08389 | 0.486 |
TRG_NES_CRM1_1 | 602 | 614 | PF08389 | 0.477 |
TRG_NLS_MonoCore_2 | 258 | 263 | PF00514 | 0.388 |
TRG_NLS_MonoExtN_4 | 256 | 263 | PF00514 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 191 | 195 | PF00026 | 0.454 |
TRG_Pf-PMV_PEXEL_1 | 220 | 225 | PF00026 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 537 | 542 | PF00026 | 0.698 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I401 | Leptomonas seymouri | 66% | 99% |
A0A1X0NSB4 | Trypanosomatidae | 46% | 100% |
A0A3R7NUR2 | Trypanosoma rangeli | 51% | 100% |
A0A3S7X625 | Leishmania donovani | 86% | 100% |
A4I8H3 | Leishmania infantum | 86% | 100% |
D0AAP5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9B3D3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q4S3 | Leishmania major | 85% | 100% |