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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4IDN8
Term | Name | Level | Count |
---|---|---|---|
GO:0006355 | regulation of DNA-templated transcription | 6 | 1 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051252 | regulation of RNA metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 1 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043169 | cation binding | 3 | 2 |
GO:0046872 | metal ion binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 106 | 110 | PF00656 | 0.579 |
CLV_C14_Caspase3-7 | 278 | 282 | PF00656 | 0.596 |
CLV_C14_Caspase3-7 | 417 | 421 | PF00656 | 0.574 |
CLV_C14_Caspase3-7 | 484 | 488 | PF00656 | 0.553 |
CLV_NRD_NRD_1 | 250 | 252 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 329 | 331 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.446 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.483 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 603 | 605 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 610 | 612 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 646 | 648 | PF00675 | 0.460 |
CLV_PCSK_FUR_1 | 644 | 648 | PF00082 | 0.543 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 329 | 331 | PF00082 | 0.277 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.172 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 531 | 533 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 610 | 612 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 646 | 648 | PF00082 | 0.456 |
CLV_PCSK_PC1ET2_1 | 146 | 148 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 252 | 254 | PF00082 | 0.498 |
CLV_PCSK_PC1ET2_1 | 496 | 498 | PF00082 | 0.696 |
CLV_PCSK_PC7_1 | 527 | 533 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 191 | 195 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.455 |
DEG_APCC_DBOX_1 | 329 | 337 | PF00400 | 0.487 |
DEG_APCC_DBOX_1 | 5 | 13 | PF00400 | 0.355 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.416 |
DEG_SCF_FBW7_1 | 50 | 56 | PF00400 | 0.700 |
DEG_SPOP_SBC_1 | 157 | 161 | PF00917 | 0.587 |
DOC_ANK_TNKS_1 | 544 | 551 | PF00023 | 0.420 |
DOC_CKS1_1 | 288 | 293 | PF01111 | 0.519 |
DOC_CKS1_1 | 50 | 55 | PF01111 | 0.609 |
DOC_CYCLIN_yCln2_LP_2 | 288 | 294 | PF00134 | 0.450 |
DOC_MAPK_gen_1 | 565 | 574 | PF00069 | 0.574 |
DOC_PP2B_LxvP_1 | 186 | 189 | PF13499 | 0.625 |
DOC_PP2B_LxvP_1 | 314 | 317 | PF13499 | 0.487 |
DOC_PP2B_LxvP_1 | 590 | 593 | PF13499 | 0.512 |
DOC_PP4_FxxP_1 | 229 | 232 | PF00568 | 0.454 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.783 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.758 |
LIG_14-3-3_CanoR_1 | 176 | 181 | PF00244 | 0.699 |
LIG_14-3-3_CanoR_1 | 214 | 221 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 251 | 260 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 29 | 34 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 296 | 304 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 567 | 575 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 646 | 651 | PF00244 | 0.537 |
LIG_Actin_WH2_2 | 331 | 348 | PF00022 | 0.487 |
LIG_CtBP_PxDLS_1 | 425 | 429 | PF00389 | 0.565 |
LIG_deltaCOP1_diTrp_1 | 577 | 580 | PF00928 | 0.522 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.608 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.653 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.537 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.676 |
LIG_FHA_1 | 613 | 619 | PF00498 | 0.513 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.363 |
LIG_FHA_2 | 482 | 488 | PF00498 | 0.565 |
LIG_FHA_2 | 50 | 56 | PF00498 | 0.525 |
LIG_GBD_Chelix_1 | 475 | 483 | PF00786 | 0.528 |
LIG_LIR_Gen_1 | 569 | 576 | PF02991 | 0.520 |
LIG_LIR_Gen_1 | 577 | 586 | PF02991 | 0.444 |
LIG_LIR_Gen_1 | 594 | 603 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 617 | 627 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 569 | 574 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 577 | 583 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 594 | 600 | PF02991 | 0.431 |
LIG_NRBOX | 478 | 484 | PF00104 | 0.537 |
LIG_SH2_NCK_1 | 597 | 601 | PF00017 | 0.501 |
LIG_SH2_PTP2 | 341 | 344 | PF00017 | 0.398 |
LIG_SH2_SRC | 247 | 250 | PF00017 | 0.414 |
LIG_SH2_SRC | 341 | 344 | PF00017 | 0.470 |
LIG_SH2_SRC | 597 | 600 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 38 | 42 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.377 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.546 |
LIG_SH3_3 | 264 | 270 | PF00018 | 0.322 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.552 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.628 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.680 |
LIG_SUMO_SIM_par_1 | 581 | 587 | PF11976 | 0.562 |
LIG_TRAF2_1 | 593 | 596 | PF00917 | 0.546 |
MOD_CDC14_SPxK_1 | 404 | 407 | PF00782 | 0.568 |
MOD_CDK_SPK_2 | 401 | 406 | PF00069 | 0.527 |
MOD_CDK_SPK_2 | 44 | 49 | PF00069 | 0.553 |
MOD_CDK_SPxK_1 | 401 | 407 | PF00069 | 0.572 |
MOD_CDK_SPxxK_3 | 158 | 165 | PF00069 | 0.587 |
MOD_CDK_SPxxK_3 | 443 | 450 | PF00069 | 0.423 |
MOD_CDK_SPxxK_3 | 488 | 495 | PF00069 | 0.679 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.586 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.660 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.699 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.587 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.572 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.745 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.369 |
MOD_CK2_1 | 312 | 318 | PF00069 | 0.555 |
MOD_CK2_1 | 581 | 587 | PF00069 | 0.420 |
MOD_DYRK1A_RPxSP_1 | 44 | 48 | PF00069 | 0.514 |
MOD_DYRK1A_RPxSP_1 | 49 | 53 | PF00069 | 0.556 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.623 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.734 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.717 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.703 |
MOD_GlcNHglycan | 196 | 200 | PF01048 | 0.662 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.505 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.428 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.531 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.728 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.514 |
MOD_GlcNHglycan | 533 | 537 | PF01048 | 0.530 |
MOD_GlcNHglycan | 54 | 58 | PF01048 | 0.649 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.544 |
MOD_GlcNHglycan | 611 | 614 | PF01048 | 0.646 |
MOD_GlcNHglycan | 660 | 663 | PF01048 | 0.596 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.795 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.716 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.641 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.695 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.712 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.719 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.632 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.670 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.513 |
MOD_GSK3_1 | 477 | 484 | PF00069 | 0.488 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.710 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.575 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.751 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.674 |
MOD_LATS_1 | 174 | 180 | PF00433 | 0.608 |
MOD_LATS_1 | 249 | 255 | PF00433 | 0.426 |
MOD_LATS_1 | 294 | 300 | PF00433 | 0.512 |
MOD_N-GLC_1 | 440 | 445 | PF02516 | 0.515 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.498 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.459 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.534 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.543 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.550 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.571 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.496 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.465 |
MOD_NEK2_2 | 550 | 555 | PF00069 | 0.495 |
MOD_PIKK_1 | 124 | 130 | PF00454 | 0.655 |
MOD_PIKK_1 | 420 | 426 | PF00454 | 0.563 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.510 |
MOD_PK_1 | 646 | 652 | PF00069 | 0.470 |
MOD_PKA_1 | 251 | 257 | PF00069 | 0.451 |
MOD_PKA_1 | 406 | 412 | PF00069 | 0.516 |
MOD_PKA_1 | 531 | 537 | PF00069 | 0.526 |
MOD_PKA_1 | 646 | 652 | PF00069 | 0.535 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.573 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.682 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.374 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.499 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.741 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.517 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.575 |
MOD_PKA_2 | 609 | 615 | PF00069 | 0.598 |
MOD_PKA_2 | 646 | 652 | PF00069 | 0.536 |
MOD_PKA_2 | 91 | 97 | PF00069 | 0.671 |
MOD_PKB_1 | 644 | 652 | PF00069 | 0.538 |
MOD_Plk_1 | 550 | 556 | PF00069 | 0.568 |
MOD_Plk_2-3 | 386 | 392 | PF00069 | 0.533 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.377 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.414 |
MOD_Plk_4 | 323 | 329 | PF00069 | 0.457 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.443 |
MOD_Plk_4 | 570 | 576 | PF00069 | 0.549 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.562 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.753 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.628 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.508 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.743 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.711 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.630 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.656 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.539 |
MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.655 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.761 |
TRG_DiLeu_BaEn_1 | 577 | 582 | PF01217 | 0.298 |
TRG_ENDOCYTIC_2 | 597 | 600 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 619 | 622 | PF00928 | 0.506 |
TRG_ER_diArg_1 | 328 | 330 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 405 | 407 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 494 | 497 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 499 | 502 | PF00400 | 0.648 |
TRG_ER_diArg_1 | 545 | 548 | PF00400 | 0.670 |
TRG_ER_diArg_1 | 644 | 647 | PF00400 | 0.468 |
TRG_NLS_MonoExtC_3 | 494 | 499 | PF00514 | 0.694 |
TRG_NLS_MonoExtN_4 | 492 | 499 | PF00514 | 0.693 |
TRG_Pf-PMV_PEXEL_1 | 547 | 551 | PF00026 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 616 | 620 | PF00026 | 0.558 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IA05 | Leptomonas seymouri | 55% | 79% |
A0A1X0P0C1 | Trypanosomatidae | 31% | 100% |
A0A3Q8IHQ6 | Leishmania donovani | 98% | 81% |
A0A422P586 | Trypanosoma rangeli | 32% | 100% |
A4HPX7 | Leishmania braziliensis | 71% | 100% |
D0A4C4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9ATP3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4Q0V5 | Leishmania major | 91% | 100% |
V5BKJ9 | Trypanosoma cruzi | 34% | 100% |