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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 16 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: A0A3S7X6K2
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 17 |
GO:0003824 | catalytic activity | 1 | 17 |
GO:0005488 | binding | 1 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0016462 | pyrophosphatase activity | 5 | 17 |
GO:0016787 | hydrolase activity | 2 | 17 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 17 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 17 |
GO:0016887 | ATP hydrolysis activity | 7 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.658 |
CLV_C14_Caspase3-7 | 381 | 385 | PF00656 | 0.741 |
CLV_C14_Caspase3-7 | 410 | 414 | PF00656 | 0.505 |
CLV_C14_Caspase3-7 | 455 | 459 | PF00656 | 0.784 |
CLV_C14_Caspase3-7 | 58 | 62 | PF00656 | 0.598 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.543 |
CLV_PCSK_FUR_1 | 437 | 441 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.285 |
CLV_PCSK_KEX2_1 | 382 | 384 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 351 | 353 | PF00082 | 0.322 |
CLV_PCSK_PC1ET2_1 | 382 | 384 | PF00082 | 0.401 |
CLV_PCSK_PC1ET2_1 | 507 | 509 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.353 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 370 | 374 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 83 | 87 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.477 |
CLV_Separin_Metazoa | 645 | 649 | PF03568 | 0.557 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.405 |
DOC_CYCLIN_RxL_1 | 192 | 203 | PF00134 | 0.619 |
DOC_CYCLIN_RxL_1 | 259 | 269 | PF00134 | 0.597 |
DOC_CYCLIN_yCln2_LP_2 | 296 | 302 | PF00134 | 0.531 |
DOC_CYCLIN_yCln2_LP_2 | 399 | 405 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 351 | 359 | PF00069 | 0.485 |
DOC_PP1_RVXF_1 | 260 | 267 | PF00149 | 0.754 |
DOC_PP2B_LxvP_1 | 106 | 109 | PF13499 | 0.688 |
DOC_SPAK_OSR1_1 | 376 | 380 | PF12202 | 0.578 |
DOC_SPAK_OSR1_1 | 97 | 101 | PF12202 | 0.680 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.365 |
DOC_USP7_MATH_1 | 599 | 603 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 615 | 619 | PF00917 | 0.757 |
DOC_USP7_UBL2_3 | 313 | 317 | PF12436 | 0.554 |
DOC_USP7_UBL2_3 | 378 | 382 | PF12436 | 0.595 |
DOC_USP7_UBL2_3 | 503 | 507 | PF12436 | 0.757 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 623 | 628 | PF00397 | 0.520 |
LIG_14-3-3_CanoR_1 | 140 | 147 | PF00244 | 0.781 |
LIG_14-3-3_CanoR_1 | 148 | 152 | PF00244 | 0.767 |
LIG_14-3-3_CanoR_1 | 361 | 369 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 52 | 57 | PF00244 | 0.634 |
LIG_14-3-3_CanoR_1 | 574 | 584 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 83 | 93 | PF00244 | 0.607 |
LIG_Actin_WH2_2 | 134 | 150 | PF00022 | 0.736 |
LIG_Actin_WH2_2 | 3 | 19 | PF00022 | 0.462 |
LIG_Actin_WH2_2 | 538 | 553 | PF00022 | 0.637 |
LIG_BRCT_BRCA1_1 | 294 | 298 | PF00533 | 0.511 |
LIG_BRCT_BRCA1_1 | 373 | 377 | PF00533 | 0.636 |
LIG_BRCT_BRCA1_1 | 63 | 67 | PF00533 | 0.701 |
LIG_CSL_BTD_1 | 44 | 47 | PF09270 | 0.668 |
LIG_eIF4E_1 | 253 | 259 | PF01652 | 0.612 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.689 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.713 |
LIG_FHA_1 | 16 | 22 | PF00498 | 0.426 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.376 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.606 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.801 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.533 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.470 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.514 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.609 |
LIG_FHA_1 | 605 | 611 | PF00498 | 0.770 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.651 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.649 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.759 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.679 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.572 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.737 |
LIG_FHA_2 | 453 | 459 | PF00498 | 0.821 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.733 |
LIG_FHA_2 | 637 | 643 | PF00498 | 0.543 |
LIG_LIR_Apic_2 | 315 | 321 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 102 | 113 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 125 | 134 | PF02991 | 0.635 |
LIG_LIR_Gen_1 | 2 | 12 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 292 | 300 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 125 | 129 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 189 | 193 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 242 | 246 | PF02991 | 0.670 |
LIG_LIR_Nem_3 | 292 | 296 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.512 |
LIG_MLH1_MIPbox_1 | 294 | 298 | PF16413 | 0.511 |
LIG_NRBOX | 326 | 332 | PF00104 | 0.423 |
LIG_NRBOX | 589 | 595 | PF00104 | 0.558 |
LIG_Pex14_2 | 293 | 297 | PF04695 | 0.473 |
LIG_Pex14_2 | 373 | 377 | PF04695 | 0.636 |
LIG_PTB_Apo_2 | 6 | 13 | PF02174 | 0.399 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.664 |
LIG_SH2_CRK | 255 | 259 | PF00017 | 0.550 |
LIG_SH2_CRK | 318 | 322 | PF00017 | 0.599 |
LIG_SH2_CRK | 332 | 336 | PF00017 | 0.408 |
LIG_SH2_NCK_1 | 318 | 322 | PF00017 | 0.629 |
LIG_SH2_SRC | 318 | 321 | PF00017 | 0.623 |
LIG_SH2_STAP1 | 119 | 123 | PF00017 | 0.672 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.359 |
LIG_SH2_STAT3 | 253 | 256 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 126 | 129 | PF00017 | 0.658 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.608 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.414 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 407 | 410 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 576 | 579 | PF00017 | 0.597 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.593 |
LIG_SH3_1 | 318 | 324 | PF00018 | 0.627 |
LIG_SH3_2 | 321 | 326 | PF14604 | 0.547 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.605 |
LIG_SH3_3 | 318 | 324 | PF00018 | 0.543 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.670 |
LIG_SUMO_SIM_anti_2 | 641 | 648 | PF11976 | 0.554 |
LIG_TRAF2_1 | 175 | 178 | PF00917 | 0.680 |
LIG_TRAF2_1 | 364 | 367 | PF00917 | 0.511 |
LIG_TRAF2_1 | 461 | 464 | PF00917 | 0.809 |
LIG_TRAF2_1 | 639 | 642 | PF00917 | 0.586 |
LIG_TYR_ITIM | 103 | 108 | PF00017 | 0.648 |
LIG_TYR_ITIM | 241 | 246 | PF00017 | 0.571 |
LIG_UBA3_1 | 180 | 187 | PF00899 | 0.612 |
LIG_UBA3_1 | 304 | 313 | PF00899 | 0.573 |
MOD_CDC14_SPxK_1 | 132 | 135 | PF00782 | 0.708 |
MOD_CDK_SPxK_1 | 129 | 135 | PF00069 | 0.699 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.384 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.759 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.653 |
MOD_CK1_1 | 394 | 400 | PF00069 | 0.609 |
MOD_CK1_1 | 451 | 457 | PF00069 | 0.775 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.685 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.635 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.674 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.691 |
MOD_CK2_1 | 361 | 367 | PF00069 | 0.452 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.740 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.793 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.735 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.634 |
MOD_CK2_1 | 623 | 629 | PF00069 | 0.551 |
MOD_CK2_1 | 636 | 642 | PF00069 | 0.539 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.442 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.397 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.588 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.443 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.496 |
MOD_GlcNHglycan | 616 | 620 | PF01048 | 0.550 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.520 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.700 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.426 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.492 |
MOD_GSK3_1 | 448 | 455 | PF00069 | 0.767 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.750 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.565 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.679 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.618 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.755 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.674 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.646 |
MOD_LATS_1 | 167 | 173 | PF00433 | 0.610 |
MOD_N-GLC_1 | 117 | 122 | PF02516 | 0.473 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.473 |
MOD_N-GLC_1 | 469 | 474 | PF02516 | 0.595 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.486 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.443 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.727 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.715 |
MOD_NEK2_1 | 33 | 38 | PF00069 | 0.369 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.492 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.476 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.637 |
MOD_NEK2_2 | 176 | 181 | PF00069 | 0.620 |
MOD_NEK2_2 | 553 | 558 | PF00069 | 0.535 |
MOD_NEK2_2 | 63 | 68 | PF00069 | 0.561 |
MOD_NEK2_2 | 78 | 83 | PF00069 | 0.686 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.656 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.720 |
MOD_PIKK_1 | 494 | 500 | PF00454 | 0.790 |
MOD_PK_1 | 104 | 110 | PF00069 | 0.618 |
MOD_PKA_1 | 507 | 513 | PF00069 | 0.731 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.724 |
MOD_PKA_2 | 147 | 153 | PF00069 | 0.717 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.723 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.610 |
MOD_Plk_1 | 615 | 621 | PF00069 | 0.648 |
MOD_Plk_2-3 | 458 | 464 | PF00069 | 0.783 |
MOD_Plk_2-3 | 589 | 595 | PF00069 | 0.591 |
MOD_Plk_2-3 | 636 | 642 | PF00069 | 0.599 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.729 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.610 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.472 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.675 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.609 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.667 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.643 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.709 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.786 |
MOD_ProDKin_1 | 623 | 629 | PF00069 | 0.519 |
MOD_SUMO_for_1 | 420 | 423 | PF00179 | 0.643 |
MOD_SUMO_rev_2 | 237 | 246 | PF00179 | 0.670 |
MOD_SUMO_rev_2 | 309 | 315 | PF00179 | 0.546 |
MOD_SUMO_rev_2 | 99 | 106 | PF00179 | 0.632 |
TRG_DiLeu_BaEn_1 | 589 | 594 | PF01217 | 0.631 |
TRG_DiLeu_BaLyEn_6 | 254 | 259 | PF01217 | 0.612 |
TRG_DiLeu_BaLyEn_6 | 300 | 305 | PF01217 | 0.612 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.566 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.647 |
TRG_ENDOCYTIC_2 | 243 | 246 | PF00928 | 0.610 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.396 |
TRG_NES_CRM1_1 | 136 | 149 | PF08389 | 0.684 |
TRG_NES_CRM1_1 | 367 | 381 | PF08389 | 0.628 |
TRG_NES_CRM1_1 | 99 | 112 | PF08389 | 0.563 |
TRG_NLS_MonoExtN_4 | 261 | 266 | PF00514 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 252 | 256 | PF00026 | 0.312 |
TRG_Pf-PMV_PEXEL_1 | 513 | 518 | PF00026 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 591 | 595 | PF00026 | 0.409 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4V2 | Leptomonas seymouri | 59% | 98% |
A0A0S4JAD3 | Bodo saltans | 32% | 100% |
A0A1X0NTT2 | Trypanosomatidae | 28% | 97% |
A0A1X0P2Y3 | Trypanosomatidae | 28% | 100% |
A0A1X0P9I4 | Trypanosomatidae | 29% | 81% |
A0A422NUH1 | Trypanosoma rangeli | 29% | 97% |
A0A422P3P3 | Trypanosoma rangeli | 30% | 100% |
A4HLH5 | Leishmania braziliensis | 73% | 96% |
A4I8Y5 | Leishmania infantum | 100% | 100% |
C9ZQW4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZSJ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 98% |
D0A1W6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 91% |
E9B3V4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q470 | Leishmania major | 93% | 100% |
V5DQN5 | Trypanosoma cruzi | 31% | 100% |