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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 2 |
GO:0097014 | ciliary plasm | 5 | 2 |
GO:0099568 | cytoplasmic region | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q741
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 15 |
GO:0003824 | catalytic activity | 1 | 15 |
GO:0005488 | binding | 1 | 15 |
GO:0005524 | ATP binding | 5 | 15 |
GO:0016462 | pyrophosphatase activity | 5 | 15 |
GO:0016787 | hydrolase activity | 2 | 15 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 15 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 15 |
GO:0016887 | ATP hydrolysis activity | 7 | 15 |
GO:0017076 | purine nucleotide binding | 4 | 15 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 15 |
GO:0030554 | adenyl nucleotide binding | 5 | 15 |
GO:0032553 | ribonucleotide binding | 3 | 15 |
GO:0032555 | purine ribonucleotide binding | 4 | 15 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 15 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 15 |
GO:0036094 | small molecule binding | 2 | 15 |
GO:0043167 | ion binding | 2 | 15 |
GO:0043168 | anion binding | 3 | 15 |
GO:0097159 | organic cyclic compound binding | 2 | 15 |
GO:0097367 | carbohydrate derivative binding | 2 | 15 |
GO:1901265 | nucleoside phosphate binding | 3 | 15 |
GO:1901363 | heterocyclic compound binding | 2 | 15 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 158 | 162 | PF00656 | 0.502 |
CLV_C14_Caspase3-7 | 638 | 642 | PF00656 | 0.283 |
CLV_C14_Caspase3-7 | 662 | 666 | PF00656 | 0.283 |
CLV_C14_Caspase3-7 | 688 | 692 | PF00656 | 0.402 |
CLV_C14_Caspase3-7 | 738 | 742 | PF00656 | 0.395 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 702 | 704 | PF00675 | 0.263 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.374 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.507 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 702 | 704 | PF00082 | 0.316 |
CLV_PCSK_PC1ET2_1 | 216 | 218 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 525 | 527 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 142 | 146 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.246 |
CLV_PCSK_SKI1_1 | 585 | 589 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 621 | 625 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 675 | 679 | PF00082 | 0.359 |
DEG_APCC_DBOX_1 | 199 | 207 | PF00400 | 0.376 |
DEG_APCC_DBOX_1 | 449 | 457 | PF00400 | 0.427 |
DEG_COP1_1 | 158 | 167 | PF00400 | 0.434 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.476 |
DEG_SCF_TRCP1_1 | 270 | 275 | PF00400 | 0.461 |
DEG_SPOP_SBC_1 | 246 | 250 | PF00917 | 0.483 |
DOC_CDC14_PxL_1 | 705 | 713 | PF14671 | 0.436 |
DOC_CYCLIN_yClb1_LxF_4 | 675 | 681 | PF00134 | 0.333 |
DOC_MAPK_DCC_7 | 44 | 53 | PF00069 | 0.412 |
DOC_MAPK_gen_1 | 44 | 53 | PF00069 | 0.512 |
DOC_MAPK_gen_1 | 525 | 531 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 674 | 681 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 696 | 706 | PF00069 | 0.283 |
DOC_MAPK_MEF2A_6 | 184 | 192 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 46 | 55 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 628 | 636 | PF00069 | 0.283 |
DOC_MAPK_MEF2A_6 | 699 | 708 | PF00069 | 0.283 |
DOC_PP1_RVXF_1 | 323 | 330 | PF00149 | 0.473 |
DOC_PP2B_LxvP_1 | 436 | 439 | PF13499 | 0.476 |
DOC_PP2B_LxvP_1 | 569 | 572 | PF13499 | 0.334 |
DOC_SPAK_OSR1_1 | 526 | 530 | PF12202 | 0.510 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.422 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.381 |
DOC_USP7_MATH_1 | 581 | 585 | PF00917 | 0.257 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.346 |
DOC_USP7_MATH_1 | 764 | 768 | PF00917 | 0.331 |
DOC_USP7_UBL2_3 | 15 | 19 | PF12436 | 0.658 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 567 | 572 | PF00397 | 0.364 |
DOC_WW_Pin1_4 | 628 | 633 | PF00397 | 0.359 |
LIG_14-3-3_CanoR_1 | 142 | 147 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 178 | 182 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 191 | 197 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 297 | 303 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 355 | 361 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 383 | 389 | PF00244 | 0.368 |
LIG_14-3-3_CanoR_1 | 408 | 414 | PF00244 | 0.300 |
LIG_14-3-3_CanoR_1 | 502 | 507 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 513 | 521 | PF00244 | 0.510 |
LIG_14-3-3_CanoR_1 | 649 | 657 | PF00244 | 0.249 |
LIG_14-3-3_CanoR_1 | 714 | 722 | PF00244 | 0.391 |
LIG_Actin_WH2_2 | 442 | 459 | PF00022 | 0.565 |
LIG_BRCT_BRCA1_1 | 560 | 564 | PF00533 | 0.404 |
LIG_deltaCOP1_diTrp_1 | 172 | 177 | PF00928 | 0.493 |
LIG_deltaCOP1_diTrp_1 | 554 | 562 | PF00928 | 0.460 |
LIG_deltaCOP1_diTrp_1 | 789 | 796 | PF00928 | 0.333 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.515 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.429 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.448 |
LIG_FHA_1 | 343 | 349 | PF00498 | 0.438 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.406 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.311 |
LIG_FHA_2 | 506 | 512 | PF00498 | 0.541 |
LIG_FHA_2 | 533 | 539 | PF00498 | 0.341 |
LIG_FHA_2 | 546 | 552 | PF00498 | 0.268 |
LIG_FHA_2 | 660 | 666 | PF00498 | 0.296 |
LIG_FHA_2 | 708 | 714 | PF00498 | 0.552 |
LIG_FHA_2 | 742 | 748 | PF00498 | 0.293 |
LIG_FHA_2 | 768 | 774 | PF00498 | 0.242 |
LIG_LIR_Gen_1 | 170 | 181 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 328 | 336 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 533 | 543 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 561 | 572 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 719 | 729 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 754 | 764 | PF02991 | 0.227 |
LIG_LIR_LC3C_4 | 281 | 284 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 274 | 279 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 328 | 332 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 533 | 539 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 561 | 567 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 719 | 725 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 754 | 760 | PF02991 | 0.227 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.495 |
LIG_MYND_1 | 130 | 134 | PF01753 | 0.405 |
LIG_PCNA_yPIPBox_3 | 478 | 491 | PF02747 | 0.342 |
LIG_Pex14_1 | 173 | 177 | PF04695 | 0.486 |
LIG_SH2_CRK | 578 | 582 | PF00017 | 0.283 |
LIG_SH2_CRK | 94 | 98 | PF00017 | 0.392 |
LIG_SH2_PTP2 | 187 | 190 | PF00017 | 0.479 |
LIG_SH2_PTP2 | 705 | 708 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 705 | 708 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 735 | 738 | PF00017 | 0.227 |
LIG_SH2_STAT5 | 743 | 746 | PF00017 | 0.227 |
LIG_SH3_2 | 709 | 714 | PF14604 | 0.333 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.361 |
LIG_SH3_3 | 526 | 532 | PF00018 | 0.412 |
LIG_SH3_3 | 600 | 606 | PF00018 | 0.227 |
LIG_SH3_3 | 691 | 697 | PF00018 | 0.252 |
LIG_SH3_3 | 703 | 709 | PF00018 | 0.333 |
LIG_SUMO_SIM_anti_2 | 747 | 754 | PF11976 | 0.227 |
LIG_SUMO_SIM_par_1 | 119 | 125 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 204 | 209 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 280 | 286 | PF11976 | 0.289 |
LIG_SUMO_SIM_par_1 | 396 | 402 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 432 | 437 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 468 | 477 | PF11976 | 0.451 |
LIG_TRAF2_1 | 670 | 673 | PF00917 | 0.265 |
LIG_TRFH_1 | 567 | 571 | PF08558 | 0.350 |
LIG_TYR_ITIM | 185 | 190 | PF00017 | 0.456 |
LIG_TYR_ITSM | 86 | 93 | PF00017 | 0.491 |
MOD_CDK_SPK_2 | 10 | 15 | PF00069 | 0.650 |
MOD_CDK_SPxK_1 | 567 | 573 | PF00069 | 0.384 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.587 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.468 |
MOD_CK1_1 | 271 | 277 | PF00069 | 0.517 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.424 |
MOD_CK1_1 | 379 | 385 | PF00069 | 0.476 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.296 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.294 |
MOD_CK1_1 | 530 | 536 | PF00069 | 0.444 |
MOD_CK1_1 | 767 | 773 | PF00069 | 0.343 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.619 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.615 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.586 |
MOD_CK2_1 | 707 | 713 | PF00069 | 0.439 |
MOD_CK2_1 | 741 | 747 | PF00069 | 0.232 |
MOD_Cter_Amidation | 214 | 217 | PF01082 | 0.482 |
MOD_DYRK1A_RPxSP_1 | 628 | 632 | PF00069 | 0.359 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.645 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.613 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.640 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.606 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.515 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.489 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.334 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.290 |
MOD_GlcNHglycan | 439 | 442 | PF01048 | 0.395 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.434 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.439 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.423 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.500 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.539 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.640 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.676 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.405 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.343 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.326 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.536 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.448 |
MOD_GSK3_1 | 655 | 662 | PF00069 | 0.257 |
MOD_GSK3_1 | 737 | 744 | PF00069 | 0.227 |
MOD_LATS_1 | 798 | 804 | PF00433 | 0.457 |
MOD_N-GLC_1 | 567 | 572 | PF02516 | 0.480 |
MOD_N-GLC_1 | 593 | 598 | PF02516 | 0.283 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.408 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.555 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.439 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.555 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.465 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.366 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.378 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.517 |
MOD_NEK2_1 | 731 | 736 | PF00069 | 0.381 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.296 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.409 |
MOD_PIKK_1 | 480 | 486 | PF00454 | 0.320 |
MOD_PIKK_1 | 655 | 661 | PF00454 | 0.227 |
MOD_PKA_1 | 800 | 806 | PF00069 | 0.647 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.563 |
MOD_PKA_2 | 177 | 183 | PF00069 | 0.390 |
MOD_PKA_2 | 190 | 196 | PF00069 | 0.270 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.465 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.517 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.415 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.535 |
MOD_Plk_1 | 491 | 497 | PF00069 | 0.248 |
MOD_Plk_1 | 527 | 533 | PF00069 | 0.404 |
MOD_Plk_1 | 593 | 599 | PF00069 | 0.359 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.424 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.387 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.479 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.382 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.396 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.253 |
MOD_Plk_4 | 558 | 564 | PF00069 | 0.449 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.289 |
MOD_Plk_4 | 731 | 737 | PF00069 | 0.190 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.507 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.582 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.670 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.593 |
MOD_ProDKin_1 | 567 | 573 | PF00069 | 0.362 |
MOD_ProDKin_1 | 628 | 634 | PF00069 | 0.359 |
MOD_SUMO_for_1 | 14 | 17 | PF00179 | 0.510 |
MOD_SUMO_rev_2 | 209 | 218 | PF00179 | 0.604 |
MOD_SUMO_rev_2 | 538 | 548 | PF00179 | 0.388 |
MOD_SUMO_rev_2 | 672 | 677 | PF00179 | 0.226 |
TRG_ENDOCYTIC_2 | 187 | 190 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 705 | 708 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.503 |
TRG_ENDOCYTIC_2 | 94 | 97 | PF00928 | 0.471 |
TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.365 |
TRG_ER_diArg_1 | 456 | 458 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 702 | 704 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 781 | 784 | PF00400 | 0.357 |
TRG_Pf-PMV_PEXEL_1 | 621 | 625 | PF00026 | 0.359 |
TRG_Pf-PMV_PEXEL_1 | 655 | 659 | PF00026 | 0.227 |
TRG_PTS1 | 804 | 807 | PF00515 | 0.477 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2H1 | Leptomonas seymouri | 66% | 88% |
A0A1X0P1J4 | Trypanosomatidae | 49% | 100% |
A0A3Q8IS46 | Leishmania donovani | 92% | 83% |
A0A3R7M308 | Trypanosoma rangeli | 48% | 100% |
A0A3S7X0L3 | Leishmania donovani | 31% | 100% |
A4HFM9 | Leishmania braziliensis | 32% | 100% |
A4HII5 | Leishmania braziliensis | 80% | 85% |
A4I2Q7 | Leishmania infantum | 31% | 100% |
A4I5S8 | Leishmania infantum | 92% | 77% |
C9ZR48 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AD83 | Leishmania major | 31% | 100% |
E9AZ07 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 32% | 100% |
E9B124 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
P32794 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 31% | 100% |
Q07844 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 96% |
V5AUZ1 | Trypanosoma cruzi | 49% | 100% |