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: 15 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: Q4Q0H4
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 16 |
GO:0003824 | catalytic activity | 1 | 16 |
GO:0005488 | binding | 1 | 16 |
GO:0005524 | ATP binding | 5 | 16 |
GO:0016462 | pyrophosphatase activity | 5 | 16 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 16 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 16 |
GO:0016887 | ATP hydrolysis activity | 7 | 16 |
GO:0017076 | purine nucleotide binding | 4 | 16 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 16 |
GO:0030554 | adenyl nucleotide binding | 5 | 16 |
GO:0032553 | ribonucleotide binding | 3 | 16 |
GO:0032555 | purine ribonucleotide binding | 4 | 16 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 16 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 16 |
GO:0036094 | small molecule binding | 2 | 16 |
GO:0043167 | ion binding | 2 | 16 |
GO:0043168 | anion binding | 3 | 16 |
GO:0097159 | organic cyclic compound binding | 2 | 16 |
GO:0097367 | carbohydrate derivative binding | 2 | 16 |
GO:1901265 | nucleoside phosphate binding | 3 | 16 |
GO:1901363 | heterocyclic compound binding | 2 | 16 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 180 | 184 | PF00656 | 0.622 |
CLV_C14_Caspase3-7 | 460 | 464 | PF00656 | 0.773 |
CLV_C14_Caspase3-7 | 628 | 632 | PF00656 | 0.627 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.319 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.321 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 402 | 404 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 596 | 598 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 643 | 645 | PF00675 | 0.433 |
CLV_PCSK_FUR_1 | 400 | 404 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.393 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.279 |
CLV_PCSK_KEX2_1 | 402 | 404 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 596 | 598 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 322 | 324 | PF00082 | 0.324 |
CLV_PCSK_PC7_1 | 318 | 324 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 405 | 409 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 564 | 568 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 606 | 610 | PF00082 | 0.469 |
DEG_APCC_DBOX_1 | 479 | 487 | PF00400 | 0.562 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.450 |
DEG_SPOP_SBC_1 | 360 | 364 | PF00917 | 0.574 |
DEG_SPOP_SBC_1 | 457 | 461 | PF00917 | 0.758 |
DOC_CKS1_1 | 191 | 196 | PF01111 | 0.543 |
DOC_CKS1_1 | 677 | 682 | PF01111 | 0.651 |
DOC_CYCLIN_yClb1_LxF_4 | 307 | 312 | PF00134 | 0.556 |
DOC_CYCLIN_yCln2_LP_2 | 165 | 171 | PF00134 | 0.603 |
DOC_MAPK_gen_1 | 130 | 138 | PF00069 | 0.574 |
DOC_MAPK_gen_1 | 162 | 171 | PF00069 | 0.611 |
DOC_MAPK_gen_1 | 204 | 211 | PF00069 | 0.623 |
DOC_MAPK_gen_1 | 373 | 379 | PF00069 | 0.600 |
DOC_MAPK_gen_1 | 517 | 527 | PF00069 | 0.588 |
DOC_MAPK_MEF2A_6 | 162 | 171 | PF00069 | 0.617 |
DOC_MAPK_MEF2A_6 | 204 | 211 | PF00069 | 0.601 |
DOC_MAPK_MEF2A_6 | 335 | 342 | PF00069 | 0.519 |
DOC_MAPK_NFAT4_5 | 162 | 170 | PF00069 | 0.518 |
DOC_PP1_RVXF_1 | 307 | 313 | PF00149 | 0.553 |
DOC_PP1_RVXF_1 | 372 | 379 | PF00149 | 0.595 |
DOC_PP1_RVXF_1 | 615 | 621 | PF00149 | 0.631 |
DOC_PP2B_LxvP_1 | 165 | 168 | PF13499 | 0.618 |
DOC_PP2B_LxvP_1 | 2 | 5 | PF13499 | 0.565 |
DOC_PP2B_LxvP_1 | 99 | 102 | PF13499 | 0.558 |
DOC_PP4_FxxP_1 | 75 | 78 | PF00568 | 0.576 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.398 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 416 | 420 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 464 | 468 | PF00917 | 0.762 |
DOC_USP7_UBL2_3 | 633 | 637 | PF12436 | 0.597 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 577 | 582 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 662 | 667 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 669 | 674 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 676 | 681 | PF00397 | 0.595 |
LIG_14-3-3_CanoR_1 | 130 | 135 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 15 | 19 | PF00244 | 0.402 |
LIG_14-3-3_CanoR_1 | 204 | 208 | PF00244 | 0.658 |
LIG_14-3-3_CanoR_1 | 391 | 401 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 405 | 411 | PF00244 | 0.751 |
LIG_14-3-3_CanoR_1 | 480 | 490 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 520 | 529 | PF00244 | 0.573 |
LIG_Actin_WH2_2 | 2 | 17 | PF00022 | 0.495 |
LIG_BIR_III_4 | 463 | 467 | PF00653 | 0.678 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.460 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.611 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.558 |
LIG_FHA_1 | 442 | 448 | PF00498 | 0.736 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.714 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.391 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.644 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.617 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.528 |
LIG_FHA_2 | 383 | 389 | PF00498 | 0.648 |
LIG_FHA_2 | 609 | 615 | PF00498 | 0.653 |
LIG_Integrin_RGD_1 | 347 | 349 | PF01839 | 0.265 |
LIG_LIR_Apic_2 | 140 | 145 | PF02991 | 0.677 |
LIG_LIR_Gen_1 | 206 | 214 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 365 | 376 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 528 | 536 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 672 | 680 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 206 | 211 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 349 | 355 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 365 | 371 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 46 | 50 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 528 | 532 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 672 | 677 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.634 |
LIG_NRBOX | 309 | 315 | PF00104 | 0.492 |
LIG_NRBOX | 482 | 488 | PF00104 | 0.589 |
LIG_PTB_Apo_2 | 128 | 135 | PF02174 | 0.620 |
LIG_RPA_C_Fungi | 17 | 29 | PF08784 | 0.476 |
LIG_RPA_C_Fungi | 368 | 380 | PF08784 | 0.336 |
LIG_SH2_CRK | 142 | 146 | PF00017 | 0.605 |
LIG_SH2_CRK | 674 | 678 | PF00017 | 0.544 |
LIG_SH2_NCK_1 | 142 | 146 | PF00017 | 0.543 |
LIG_SH2_PTP2 | 529 | 532 | PF00017 | 0.370 |
LIG_SH2_SRC | 100 | 103 | PF00017 | 0.585 |
LIG_SH2_STAP1 | 249 | 253 | PF00017 | 0.375 |
LIG_SH2_STAP1 | 97 | 101 | PF00017 | 0.471 |
LIG_SH2_STAT3 | 301 | 304 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.415 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 703 | 706 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.566 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.559 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.430 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.525 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.446 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.502 |
LIG_SH3_3 | 398 | 404 | PF00018 | 0.726 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.580 |
LIG_SH3_4 | 429 | 436 | PF00018 | 0.584 |
LIG_SUMO_SIM_anti_2 | 495 | 504 | PF11976 | 0.411 |
LIG_SUMO_SIM_anti_2 | 53 | 58 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 137 | 143 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 500 | 506 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 55 | 62 | PF11976 | 0.318 |
LIG_SUMO_SIM_par_1 | 587 | 594 | PF11976 | 0.571 |
LIG_TRAF2_1 | 364 | 367 | PF00917 | 0.663 |
LIG_TRAF2_1 | 440 | 443 | PF00917 | 0.558 |
LIG_UBA3_1 | 110 | 117 | PF00899 | 0.435 |
LIG_UBA3_1 | 135 | 144 | PF00899 | 0.451 |
LIG_WRC_WIRS_1 | 158 | 163 | PF05994 | 0.429 |
LIG_WRC_WIRS_1 | 342 | 347 | PF05994 | 0.381 |
MOD_CDK_SPK_2 | 190 | 195 | PF00069 | 0.399 |
MOD_CDK_SPK_2 | 256 | 261 | PF00069 | 0.349 |
MOD_CDK_SPxxK_3 | 190 | 197 | PF00069 | 0.408 |
MOD_CDK_SPxxK_3 | 577 | 584 | PF00069 | 0.523 |
MOD_CDK_SPxxK_3 | 662 | 669 | PF00069 | 0.461 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.539 |
MOD_CK1_1 | 437 | 443 | PF00069 | 0.638 |
MOD_CK1_1 | 467 | 473 | PF00069 | 0.712 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.420 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.698 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.536 |
MOD_CK2_1 | 122 | 128 | PF00069 | 0.507 |
MOD_CK2_1 | 13 | 19 | PF00069 | 0.616 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.485 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.596 |
MOD_CK2_1 | 437 | 443 | PF00069 | 0.740 |
MOD_Cter_Amidation | 320 | 323 | PF01082 | 0.381 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.573 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.636 |
MOD_GlcNHglycan | 418 | 422 | PF01048 | 0.620 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.632 |
MOD_GlcNHglycan | 575 | 579 | PF01048 | 0.710 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.689 |
MOD_GlcNHglycan | 700 | 703 | PF01048 | 0.386 |
MOD_GlcNHglycan | 709 | 712 | PF01048 | 0.489 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.664 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.505 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.295 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.594 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.658 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.734 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.595 |
MOD_N-GLC_1 | 130 | 135 | PF02516 | 0.584 |
MOD_N-GLC_1 | 705 | 710 | PF02516 | 0.528 |
MOD_N-GLC_2 | 593 | 595 | PF02516 | 0.523 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.553 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.553 |
MOD_NEK2_1 | 264 | 269 | PF00069 | 0.429 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.559 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.344 |
MOD_NEK2_1 | 574 | 579 | PF00069 | 0.603 |
MOD_NEK2_1 | 625 | 630 | PF00069 | 0.533 |
MOD_NEK2_2 | 157 | 162 | PF00069 | 0.427 |
MOD_NEK2_2 | 203 | 208 | PF00069 | 0.418 |
MOD_NEK2_2 | 341 | 346 | PF00069 | 0.225 |
MOD_NEK2_2 | 95 | 100 | PF00069 | 0.436 |
MOD_PIKK_1 | 409 | 415 | PF00454 | 0.737 |
MOD_PIKK_1 | 429 | 435 | PF00454 | 0.583 |
MOD_PIKK_1 | 660 | 666 | PF00454 | 0.489 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.493 |
MOD_PKA_2 | 203 | 209 | PF00069 | 0.556 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.381 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.687 |
MOD_PKA_2 | 479 | 485 | PF00069 | 0.370 |
MOD_PKB_1 | 403 | 411 | PF00069 | 0.597 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.576 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.367 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.486 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.495 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.447 |
MOD_Plk_4 | 286 | 292 | PF00069 | 0.393 |
MOD_Plk_4 | 467 | 473 | PF00069 | 0.618 |
MOD_Plk_4 | 482 | 488 | PF00069 | 0.482 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.355 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.531 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.416 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.497 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.464 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.584 |
MOD_ProDKin_1 | 577 | 583 | PF00069 | 0.522 |
MOD_ProDKin_1 | 662 | 668 | PF00069 | 0.455 |
MOD_ProDKin_1 | 669 | 675 | PF00069 | 0.628 |
MOD_ProDKin_1 | 676 | 682 | PF00069 | 0.479 |
MOD_SUMO_rev_2 | 626 | 634 | PF00179 | 0.478 |
TRG_DiLeu_BaEn_1 | 19 | 24 | PF01217 | 0.470 |
TRG_DiLeu_BaEn_1 | 366 | 371 | PF01217 | 0.467 |
TRG_DiLeu_BaEn_1 | 531 | 536 | PF01217 | 0.523 |
TRG_DiLeu_BaEn_4 | 366 | 372 | PF01217 | 0.468 |
TRG_DiLeu_LyEn_5 | 19 | 24 | PF01217 | 0.470 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.552 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.657 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 571 | 574 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 674 | 677 | PF00928 | 0.507 |
TRG_ENDOCYTIC_2 | 85 | 88 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 96 | 99 | PF00928 | 0.679 |
TRG_ER_diArg_1 | 209 | 212 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.336 |
TRG_ER_diArg_1 | 390 | 393 | PF00400 | 0.511 |
TRG_ER_diArg_1 | 399 | 402 | PF00400 | 0.636 |
TRG_Pf-PMV_PEXEL_1 | 116 | 120 | PF00026 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 606 | 610 | PF00026 | 0.495 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P906 | Leptomonas seymouri | 46% | 98% |
A0A3Q8IC80 | Leishmania donovani | 29% | 100% |
A0A3Q8IC95 | Leishmania donovani | 28% | 100% |
A0A3Q8IHZ0 | Leishmania donovani | 90% | 100% |
A0A422NUH1 | Trypanosoma rangeli | 31% | 100% |
A4HCE5 | Leishmania braziliensis | 27% | 100% |
A4HZW7 | Leishmania infantum | 29% | 100% |
A4IDZ9 | Leishmania infantum | 90% | 100% |
E9AU21 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
E9AVS5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AVS6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 99% |
Q4QBQ3 | Leishmania major | 28% | 98% |
Q4QBQ4 | Leishmania major | 28% | 100% |
V5DMJ8 | Trypanosoma cruzi | 28% | 100% |