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: 3 |
Silverman et al. | no | yes: 3 |
Pissara et al. | yes | yes: 12 |
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: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0043226 | organelle | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7X2D2
Term | Name | Level | Count |
---|---|---|---|
GO:0000413 | protein peptidyl-prolyl isomerization | 7 | 1 |
GO:0006457 | protein folding | 2 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018208 | peptidyl-proline modification | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0061077 | chaperone-mediated protein folding | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0044183 | protein folding chaperone | 1 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:0140662 | ATP-dependent protein folding chaperone | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003755 | peptidyl-prolyl cis-trans isomerase activity | 3 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0016853 | isomerase activity | 2 | 1 |
GO:0016859 | cis-trans isomerase activity | 3 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 424 | 428 | PF00656 | 0.515 |
CLV_C14_Caspase3-7 | 455 | 459 | PF00656 | 0.519 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.374 |
CLV_PCSK_KEX2_1 | 387 | 389 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 580 | 582 | PF00082 | 0.556 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 667 | 669 | PF00082 | 0.400 |
CLV_PCSK_PC1ET2_1 | 548 | 550 | PF00082 | 0.550 |
CLV_PCSK_PC1ET2_1 | 580 | 582 | PF00082 | 0.612 |
CLV_PCSK_PC1ET2_1 | 623 | 625 | PF00082 | 0.499 |
CLV_PCSK_PC7_1 | 544 | 550 | PF00082 | 0.586 |
CLV_PCSK_PC7_1 | 576 | 582 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 358 | 362 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 663 | 667 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 706 | 710 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 717 | 721 | PF00082 | 0.512 |
DEG_APCC_DBOX_1 | 311 | 319 | PF00400 | 0.458 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.585 |
DOC_ANK_TNKS_1 | 339 | 346 | PF00023 | 0.462 |
DOC_CYCLIN_yCln2_LP_2 | 100 | 106 | PF00134 | 0.410 |
DOC_MAPK_gen_1 | 442 | 450 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 548 | 557 | PF00069 | 0.551 |
DOC_MAPK_gen_1 | 620 | 628 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 125 | 133 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 68 | 76 | PF00069 | 0.500 |
DOC_PP2B_LxvP_1 | 131 | 134 | PF13499 | 0.462 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.490 |
DOC_USP7_UBL2_3 | 256 | 260 | PF12436 | 0.402 |
DOC_USP7_UBL2_3 | 713 | 717 | PF12436 | 0.529 |
DOC_USP7_UBL2_3 | 718 | 722 | PF12436 | 0.561 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.537 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.462 |
LIG_14-3-3_CanoR_1 | 312 | 322 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 365 | 371 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 434 | 441 | PF00244 | 0.618 |
LIG_Actin_WH2_2 | 209 | 224 | PF00022 | 0.478 |
LIG_Clathr_ClatBox_1 | 420 | 424 | PF01394 | 0.524 |
LIG_deltaCOP1_diTrp_1 | 591 | 601 | PF00928 | 0.498 |
LIG_EH1_1 | 108 | 116 | PF00400 | 0.438 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.481 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.462 |
LIG_FHA_1 | 513 | 519 | PF00498 | 0.487 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.474 |
LIG_FHA_1 | 650 | 656 | PF00498 | 0.543 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.525 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.432 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.771 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.405 |
LIG_FHA_2 | 59 | 65 | PF00498 | 0.462 |
LIG_FHA_2 | 612 | 618 | PF00498 | 0.545 |
LIG_Integrin_RGD_1 | 252 | 254 | PF01839 | 0.462 |
LIG_LIR_Gen_1 | 141 | 150 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 234 | 244 | PF02991 | 0.438 |
LIG_LIR_Gen_1 | 446 | 454 | PF02991 | 0.624 |
LIG_LIR_Gen_1 | 530 | 540 | PF02991 | 0.602 |
LIG_LIR_Gen_1 | 629 | 639 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 234 | 240 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 257 | 261 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 446 | 450 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 530 | 536 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.565 |
LIG_LIR_Nem_3 | 629 | 634 | PF02991 | 0.500 |
LIG_Pex14_1 | 56 | 60 | PF04695 | 0.462 |
LIG_Pex14_2 | 720 | 724 | PF04695 | 0.575 |
LIG_Rb_pABgroove_1 | 606 | 614 | PF01858 | 0.536 |
LIG_RPA_C_Fungi | 465 | 477 | PF08784 | 0.457 |
LIG_RPA_C_Fungi | 663 | 675 | PF08784 | 0.462 |
LIG_SH2_CRK | 177 | 181 | PF00017 | 0.462 |
LIG_SH2_CRK | 672 | 676 | PF00017 | 0.410 |
LIG_SH2_GRB2like | 631 | 634 | PF00017 | 0.498 |
LIG_SH2_SRC | 631 | 634 | PF00017 | 0.476 |
LIG_SH2_SRC | 678 | 681 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 678 | 682 | PF00017 | 0.378 |
LIG_SH2_STAT3 | 474 | 477 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 171 | 174 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 631 | 634 | PF00017 | 0.498 |
LIG_SH3_3 | 656 | 662 | PF00018 | 0.505 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.470 |
LIG_SUMO_SIM_anti_2 | 288 | 294 | PF11976 | 0.462 |
LIG_SUMO_SIM_par_1 | 189 | 195 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 290 | 296 | PF11976 | 0.488 |
LIG_TRAF2_1 | 615 | 618 | PF00917 | 0.626 |
LIG_TYR_ITIM | 175 | 180 | PF00017 | 0.410 |
LIG_UBA3_1 | 114 | 121 | PF00899 | 0.378 |
LIG_UBA3_1 | 314 | 321 | PF00899 | 0.410 |
LIG_WRC_WIRS_1 | 23 | 28 | PF05994 | 0.462 |
LIG_WRC_WIRS_1 | 255 | 260 | PF05994 | 0.462 |
LIG_WW_3 | 337 | 341 | PF00397 | 0.378 |
MOD_CDK_SPxxK_3 | 427 | 434 | PF00069 | 0.489 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.471 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.498 |
MOD_CK1_1 | 542 | 548 | PF00069 | 0.551 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.463 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.432 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.496 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.545 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.658 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.626 |
MOD_CK2_1 | 531 | 537 | PF00069 | 0.542 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.475 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.639 |
MOD_Cter_Amidation | 240 | 243 | PF01082 | 0.378 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.433 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.532 |
MOD_GlcNHglycan | 378 | 382 | PF01048 | 0.461 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.471 |
MOD_GlcNHglycan | 672 | 675 | PF01048 | 0.447 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.492 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.507 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.419 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.394 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.375 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.826 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.501 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.602 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.462 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.688 |
MOD_N-GLC_1 | 372 | 377 | PF02516 | 0.410 |
MOD_N-GLC_1 | 618 | 623 | PF02516 | 0.571 |
MOD_N-GLC_1 | 649 | 654 | PF02516 | 0.527 |
MOD_N-GLC_2 | 649 | 651 | PF02516 | 0.536 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.461 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.462 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.453 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.462 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.552 |
MOD_NEK2_2 | 217 | 222 | PF00069 | 0.321 |
MOD_NEK2_2 | 539 | 544 | PF00069 | 0.532 |
MOD_NEK2_2 | 635 | 640 | PF00069 | 0.502 |
MOD_OFUCOSY | 630 | 637 | PF10250 | 0.431 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.450 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.457 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.378 |
MOD_PIKK_1 | 689 | 695 | PF00454 | 0.546 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.431 |
MOD_PKA_1 | 387 | 393 | PF00069 | 0.488 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.616 |
MOD_Plk_1 | 156 | 162 | PF00069 | 0.410 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.597 |
MOD_Plk_1 | 275 | 281 | PF00069 | 0.477 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.561 |
MOD_Plk_1 | 624 | 630 | PF00069 | 0.535 |
MOD_Plk_2-3 | 30 | 36 | PF00069 | 0.423 |
MOD_Plk_2-3 | 531 | 537 | PF00069 | 0.458 |
MOD_Plk_2-3 | 613 | 619 | PF00069 | 0.564 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.455 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.469 |
MOD_Plk_4 | 19 | 25 | PF00069 | 0.462 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.451 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.375 |
MOD_Plk_4 | 46 | 52 | PF00069 | 0.486 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.487 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.445 |
MOD_Plk_4 | 603 | 609 | PF00069 | 0.484 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.438 |
MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.535 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.462 |
MOD_SUMO_for_1 | 182 | 185 | PF00179 | 0.321 |
MOD_SUMO_for_1 | 589 | 592 | PF00179 | 0.510 |
MOD_SUMO_rev_2 | 249 | 258 | PF00179 | 0.509 |
MOD_SUMO_rev_2 | 320 | 328 | PF00179 | 0.321 |
MOD_SUMO_rev_2 | 488 | 493 | PF00179 | 0.531 |
MOD_SUMO_rev_2 | 563 | 570 | PF00179 | 0.652 |
MOD_SUMO_rev_2 | 613 | 621 | PF00179 | 0.602 |
TRG_DiLeu_BaEn_4 | 552 | 558 | PF01217 | 0.586 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 540 | 543 | PF00928 | 0.621 |
TRG_ENDOCYTIC_2 | 631 | 634 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 672 | 675 | PF00928 | 0.410 |
TRG_ER_diArg_1 | 386 | 388 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 574 | 577 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 666 | 668 | PF00400 | 0.400 |
TRG_ER_FFAT_1 | 673 | 684 | PF00635 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 260 | 264 | PF00026 | 0.433 |
TRG_Pf-PMV_PEXEL_1 | 434 | 438 | PF00026 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 92 | 97 | PF00026 | 0.462 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6E2 | Leptomonas seymouri | 71% | 94% |
A0A0S4JRE7 | Bodo saltans | 41% | 100% |
A0A3S7X203 | Leishmania donovani | 23% | 100% |
A4HGY5 | Leishmania braziliensis | 24% | 100% |
A4HHD6 | Leishmania braziliensis | 86% | 100% |
A4I4I1 | Leishmania infantum | 100% | 100% |
E9ADY2 | Leishmania major | 94% | 100% |
E9ALU9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
E9B0A4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
V5BI61 | Trypanosoma cruzi | 24% | 100% |