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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A4HMT2
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 293 | 297 | PF00656 | 0.515 |
CLV_C14_Caspase3-7 | 741 | 745 | PF00656 | 0.632 |
CLV_MEL_PAP_1 | 2 | 8 | PF00089 | 0.300 |
CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 401 | 403 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 450 | 452 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 529 | 531 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 535 | 537 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 590 | 592 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 706 | 708 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.557 |
CLV_PCSK_FUR_1 | 533 | 537 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 535 | 537 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 705 | 707 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.670 |
CLV_PCSK_PC1ET2_1 | 705 | 707 | PF00082 | 0.618 |
CLV_PCSK_PC1ET2_1 | 98 | 100 | PF00082 | 0.778 |
CLV_PCSK_PC7_1 | 84 | 90 | PF00082 | 0.548 |
CLV_PCSK_PC7_1 | 94 | 100 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 272 | 276 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.519 |
CLV_Separin_Metazoa | 364 | 368 | PF03568 | 0.547 |
DEG_APCC_DBOX_1 | 199 | 207 | PF00400 | 0.678 |
DEG_APCC_DBOX_1 | 271 | 279 | PF00400 | 0.403 |
DEG_COP1_1 | 183 | 192 | PF00400 | 0.523 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.373 |
DEG_SPOP_SBC_1 | 182 | 186 | PF00917 | 0.683 |
DEG_SPOP_SBC_1 | 439 | 443 | PF00917 | 0.722 |
DOC_ANK_TNKS_1 | 589 | 596 | PF00023 | 0.662 |
DOC_CKS1_1 | 280 | 285 | PF01111 | 0.458 |
DOC_CKS1_1 | 369 | 374 | PF01111 | 0.563 |
DOC_CYCLIN_yCln2_LP_2 | 690 | 696 | PF00134 | 0.390 |
DOC_MAPK_gen_1 | 22 | 30 | PF00069 | 0.321 |
DOC_MAPK_gen_1 | 281 | 289 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 3 | 12 | PF00069 | 0.461 |
DOC_MAPK_gen_1 | 322 | 331 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 337 | 344 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 356 | 365 | PF00069 | 0.289 |
DOC_MAPK_gen_1 | 483 | 490 | PF00069 | 0.658 |
DOC_MAPK_gen_1 | 530 | 540 | PF00069 | 0.606 |
DOC_MAPK_MEF2A_6 | 272 | 280 | PF00069 | 0.379 |
DOC_MAPK_MEF2A_6 | 281 | 289 | PF00069 | 0.493 |
DOC_MAPK_MEF2A_6 | 3 | 12 | PF00069 | 0.416 |
DOC_MAPK_NFAT4_5 | 5 | 13 | PF00069 | 0.419 |
DOC_PP1_RVXF_1 | 46 | 52 | PF00149 | 0.414 |
DOC_PP1_RVXF_1 | 7 | 13 | PF00149 | 0.431 |
DOC_PP4_FxxP_1 | 280 | 283 | PF00568 | 0.471 |
DOC_PP4_FxxP_1 | 30 | 33 | PF00568 | 0.487 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 240 | 244 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 419 | 423 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 628 | 632 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 726 | 730 | PF00917 | 0.610 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 117 | 122 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 279 | 284 | PF00397 | 0.440 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.529 |
LIG_14-3-3_CanoR_1 | 450 | 455 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 600 | 608 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 697 | 703 | PF00244 | 0.573 |
LIG_Actin_WH2_2 | 225 | 240 | PF00022 | 0.520 |
LIG_AP2alpha_2 | 687 | 689 | PF02296 | 0.656 |
LIG_Clathr_ClatBox_1 | 354 | 358 | PF01394 | 0.451 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.348 |
LIG_eIF4E_1 | 270 | 276 | PF01652 | 0.270 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.620 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.431 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.530 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.736 |
LIG_FHA_1 | 540 | 546 | PF00498 | 0.459 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.543 |
LIG_FHA_1 | 610 | 616 | PF00498 | 0.405 |
LIG_FHA_1 | 697 | 703 | PF00498 | 0.578 |
LIG_FHA_2 | 138 | 144 | PF00498 | 0.661 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.406 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.627 |
LIG_FHA_2 | 507 | 513 | PF00498 | 0.569 |
LIG_GBD_Chelix_1 | 639 | 647 | PF00786 | 0.421 |
LIG_Integrin_RGD_1 | 322 | 324 | PF01839 | 0.543 |
LIG_LIR_Apic_2 | 29 | 33 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 308 | 317 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 35 | 45 | PF02991 | 0.434 |
LIG_LIR_Gen_1 | 50 | 59 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 578 | 586 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 666 | 676 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 677 | 688 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 76 | 87 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 308 | 312 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 35 | 41 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 426 | 431 | PF02991 | 0.708 |
LIG_LIR_Nem_3 | 50 | 54 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 57 | 62 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 578 | 582 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 666 | 672 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 677 | 683 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.388 |
LIG_Rb_LxCxE_1 | 155 | 174 | PF01857 | 0.569 |
LIG_SH2_CRK | 661 | 665 | PF00017 | 0.411 |
LIG_SH2_GRB2like | 680 | 683 | PF00017 | 0.501 |
LIG_SH2_SRC | 123 | 126 | PF00017 | 0.514 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 680 | 683 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.460 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.520 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.608 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.516 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.570 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.424 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.620 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.622 |
LIG_SH3_3 | 614 | 620 | PF00018 | 0.518 |
LIG_SH3_3 | 685 | 691 | PF00018 | 0.553 |
LIG_SUMO_SIM_par_1 | 380 | 386 | PF11976 | 0.658 |
LIG_SUMO_SIM_par_1 | 392 | 397 | PF11976 | 0.669 |
LIG_TRAF2_1 | 484 | 487 | PF00917 | 0.613 |
LIG_UBA3_1 | 353 | 362 | PF00899 | 0.541 |
LIG_WRC_WIRS_1 | 27 | 32 | PF05994 | 0.573 |
MOD_CDK_SPK_2 | 279 | 284 | PF00069 | 0.440 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.517 |
MOD_CK1_1 | 166 | 172 | PF00069 | 0.685 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.622 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.669 |
MOD_CK1_1 | 441 | 447 | PF00069 | 0.724 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.598 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.489 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.572 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.514 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.461 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.623 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.628 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.438 |
MOD_CK2_1 | 481 | 487 | PF00069 | 0.639 |
MOD_CK2_1 | 628 | 634 | PF00069 | 0.558 |
MOD_CK2_1 | 716 | 722 | PF00069 | 0.624 |
MOD_Cter_Amidation | 400 | 403 | PF01082 | 0.539 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.768 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.693 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.532 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.730 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.785 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.546 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.565 |
MOD_GlcNHglycan | 470 | 473 | PF01048 | 0.599 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.566 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.420 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.575 |
MOD_GlcNHglycan | 66 | 70 | PF01048 | 0.500 |
MOD_GlcNHglycan | 676 | 679 | PF01048 | 0.522 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.541 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.637 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.775 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.715 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.724 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.484 |
MOD_GSK3_1 | 410 | 417 | PF00069 | 0.773 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.653 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.607 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.697 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.586 |
MOD_GSK3_1 | 603 | 610 | PF00069 | 0.525 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.564 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.565 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.454 |
MOD_N-GLC_1 | 423 | 428 | PF02516 | 0.708 |
MOD_N-GLC_2 | 646 | 648 | PF02516 | 0.503 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.682 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.640 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.744 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.553 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.758 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.502 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.606 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.510 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.476 |
MOD_NEK2_1 | 708 | 713 | PF00069 | 0.484 |
MOD_NEK2_2 | 380 | 385 | PF00069 | 0.732 |
MOD_NEK2_2 | 611 | 616 | PF00069 | 0.570 |
MOD_PIKK_1 | 164 | 170 | PF00454 | 0.435 |
MOD_PIKK_1 | 298 | 304 | PF00454 | 0.545 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.649 |
MOD_PIKK_1 | 539 | 545 | PF00454 | 0.483 |
MOD_PIKK_1 | 571 | 577 | PF00454 | 0.429 |
MOD_PIKK_1 | 601 | 607 | PF00454 | 0.355 |
MOD_PIKK_1 | 696 | 702 | PF00454 | 0.528 |
MOD_PKA_1 | 450 | 456 | PF00069 | 0.772 |
MOD_PKA_1 | 88 | 94 | PF00069 | 0.536 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.485 |
MOD_PKA_2 | 449 | 455 | PF00069 | 0.693 |
MOD_PKA_2 | 571 | 577 | PF00069 | 0.676 |
MOD_PKA_2 | 696 | 702 | PF00069 | 0.553 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.536 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.501 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.693 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.438 |
MOD_Plk_1 | 641 | 647 | PF00069 | 0.508 |
MOD_Plk_1 | 716 | 722 | PF00069 | 0.598 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.602 |
MOD_Plk_2-3 | 143 | 149 | PF00069 | 0.693 |
MOD_Plk_2-3 | 26 | 32 | PF00069 | 0.457 |
MOD_Plk_2-3 | 34 | 40 | PF00069 | 0.469 |
MOD_Plk_4 | 106 | 112 | PF00069 | 0.519 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.485 |
MOD_Plk_4 | 214 | 220 | PF00069 | 0.631 |
MOD_Plk_4 | 603 | 609 | PF00069 | 0.559 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.766 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.774 |
MOD_ProDKin_1 | 279 | 285 | PF00069 | 0.449 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.532 |
MOD_SUMO_rev_2 | 208 | 214 | PF00179 | 0.497 |
MOD_SUMO_rev_2 | 40 | 50 | PF00179 | 0.457 |
MOD_SUMO_rev_2 | 588 | 598 | PF00179 | 0.660 |
TRG_DiLeu_BaLyEn_6 | 349 | 354 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 597 | 602 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 661 | 664 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 680 | 683 | PF00928 | 0.546 |
TRG_ER_diArg_1 | 2 | 5 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 449 | 451 | PF00400 | 0.761 |
TRG_ER_diArg_1 | 482 | 485 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 532 | 535 | PF00400 | 0.616 |
TRG_ER_diArg_1 | 589 | 591 | PF00400 | 0.574 |
TRG_ER_diArg_1 | 706 | 708 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.434 |
TRG_Pf-PMV_PEXEL_1 | 42 | 46 | PF00026 | 0.535 |
TRG_Pf-PMV_PEXEL_1 | 600 | 605 | PF00026 | 0.603 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDF9 | Leptomonas seymouri | 68% | 100% |
A0A1X0P5J9 | Trypanosomatidae | 46% | 100% |
A0A3S7X9C0 | Leishmania donovani | 81% | 100% |
A4IBD0 | Leishmania infantum | 81% | 100% |
C9ZZ89 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AF86 | Leishmania major | 81% | 99% |
E9B6E1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
V5DUV4 | Trypanosoma cruzi | 49% | 100% |