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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AC34
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0007264 | small GTPase mediated signal transduction | 4 | 2 |
GO:0007265 | Ras protein signal transduction | 5 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016567 | protein ubiquitination | 7 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0032446 | protein modification by small protein conjugation | 6 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 2 |
GO:0005488 | binding | 1 | 7 |
GO:0008270 | zinc ion binding | 6 | 7 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 2 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0046914 | transition metal ion binding | 5 | 7 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 2 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 2 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 2 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 246 | 250 | PF00656 | 0.826 |
CLV_C14_Caspase3-7 | 252 | 256 | PF00656 | 0.779 |
CLV_C14_Caspase3-7 | 549 | 553 | PF00656 | 0.765 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.720 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.844 |
CLV_NRD_NRD_1 | 452 | 454 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 600 | 602 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 615 | 617 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 647 | 649 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 651 | 653 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 715 | 717 | PF00675 | 0.609 |
CLV_PCSK_FUR_1 | 450 | 454 | PF00082 | 0.346 |
CLV_PCSK_FUR_1 | 597 | 601 | PF00082 | 0.564 |
CLV_PCSK_FUR_1 | 648 | 652 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 597 | 599 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 600 | 602 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 615 | 617 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 647 | 649 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 650 | 652 | PF00082 | 0.576 |
CLV_PCSK_PC7_1 | 593 | 599 | PF00082 | 0.590 |
CLV_PCSK_PC7_1 | 647 | 653 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 651 | 655 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 717 | 721 | PF00082 | 0.443 |
CLV_Separin_Metazoa | 129 | 133 | PF03568 | 0.515 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.655 |
DEG_SPOP_SBC_1 | 103 | 107 | PF00917 | 0.630 |
DEG_SPOP_SBC_1 | 521 | 525 | PF00917 | 0.801 |
DEG_SPOP_SBC_1 | 96 | 100 | PF00917 | 0.703 |
DOC_CKS1_1 | 291 | 296 | PF01111 | 0.823 |
DOC_CYCLIN_yCln2_LP_2 | 170 | 176 | PF00134 | 0.677 |
DOC_CYCLIN_yCln2_LP_2 | 21 | 24 | PF00134 | 0.606 |
DOC_PP2B_LxvP_1 | 170 | 173 | PF13499 | 0.698 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.606 |
DOC_SPAK_OSR1_1 | 416 | 420 | PF12202 | 0.559 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.728 |
DOC_USP7_MATH_1 | 335 | 339 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 345 | 349 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.817 |
DOC_USP7_MATH_1 | 739 | 743 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.619 |
DOC_USP7_MATH_2 | 173 | 179 | PF00917 | 0.503 |
DOC_WW_Pin1_4 | 280 | 285 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.767 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 343 | 348 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 503 | 508 | PF00397 | 0.755 |
DOC_WW_Pin1_4 | 535 | 540 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 619 | 624 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 87 | 92 | PF00397 | 0.644 |
LIG_14-3-3_CanoR_1 | 416 | 420 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 477 | 485 | PF00244 | 0.614 |
LIG_14-3-3_CanoR_1 | 546 | 551 | PF00244 | 0.666 |
LIG_APCC_ABBA_1 | 483 | 488 | PF00400 | 0.546 |
LIG_APCC_ABBAyCdc20_2 | 482 | 488 | PF00400 | 0.546 |
LIG_APCC_ABBAyCdc20_2 | 650 | 656 | PF00400 | 0.448 |
LIG_BIR_III_2 | 179 | 183 | PF00653 | 0.622 |
LIG_BRCT_BRCA1_1 | 371 | 375 | PF00533 | 0.574 |
LIG_BRCT_BRCA1_1 | 480 | 484 | PF00533 | 0.546 |
LIG_Clathr_ClatBox_1 | 54 | 58 | PF01394 | 0.525 |
LIG_FHA_1 | 123 | 129 | PF00498 | 0.567 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.607 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.569 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.450 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.554 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.647 |
LIG_FHA_1 | 511 | 517 | PF00498 | 0.596 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.544 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.531 |
LIG_FHA_1 | 659 | 665 | PF00498 | 0.650 |
LIG_FHA_1 | 709 | 715 | PF00498 | 0.658 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.546 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.568 |
LIG_LIR_Gen_1 | 125 | 135 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 227 | 237 | PF02991 | 0.777 |
LIG_LIR_Gen_1 | 372 | 383 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 400 | 410 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 418 | 426 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 433 | 442 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 227 | 232 | PF02991 | 0.764 |
LIG_LIR_Nem_3 | 372 | 378 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 400 | 405 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 418 | 423 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 433 | 437 | PF02991 | 0.546 |
LIG_PCNA_PIPBox_1 | 689 | 698 | PF02747 | 0.537 |
LIG_PDZ_Class_1 | 738 | 743 | PF00595 | 0.545 |
LIG_SH2_CRK | 143 | 147 | PF00017 | 0.492 |
LIG_SH2_CRK | 402 | 406 | PF00017 | 0.411 |
LIG_SH2_CRK | 420 | 424 | PF00017 | 0.582 |
LIG_SH2_STAP1 | 434 | 438 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 575 | 579 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 590 | 594 | PF00017 | 0.563 |
LIG_SH2_STAT3 | 574 | 577 | PF00017 | 0.637 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.671 |
LIG_SH2_STAT5 | 384 | 387 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 657 | 660 | PF00017 | 0.645 |
LIG_SH3_1 | 344 | 350 | PF00018 | 0.795 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.831 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.800 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.643 |
LIG_SUMO_SIM_anti_2 | 125 | 132 | PF11976 | 0.533 |
LIG_SUMO_SIM_anti_2 | 488 | 495 | PF11976 | 0.545 |
LIG_SUMO_SIM_anti_2 | 661 | 666 | PF11976 | 0.640 |
LIG_SUMO_SIM_par_1 | 181 | 186 | PF11976 | 0.609 |
LIG_SUMO_SIM_par_1 | 223 | 230 | PF11976 | 0.705 |
LIG_SUMO_SIM_par_1 | 52 | 58 | PF11976 | 0.534 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.569 |
LIG_TRAF2_1 | 566 | 569 | PF00917 | 0.572 |
LIG_TRAF2_1 | 726 | 729 | PF00917 | 0.592 |
LIG_WW_3 | 211 | 215 | PF00397 | 0.647 |
MOD_CDC14_SPxK_1 | 295 | 298 | PF00782 | 0.731 |
MOD_CDC14_SPxK_1 | 346 | 349 | PF00782 | 0.733 |
MOD_CDK_SPK_2 | 327 | 332 | PF00069 | 0.714 |
MOD_CDK_SPxK_1 | 292 | 298 | PF00069 | 0.731 |
MOD_CDK_SPxK_1 | 343 | 349 | PF00069 | 0.745 |
MOD_CK1_1 | 107 | 113 | PF00069 | 0.574 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.773 |
MOD_CK1_1 | 337 | 343 | PF00069 | 0.809 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.466 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.411 |
MOD_CK1_1 | 506 | 512 | PF00069 | 0.755 |
MOD_CK1_1 | 634 | 640 | PF00069 | 0.686 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.760 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.793 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.753 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.595 |
MOD_CK2_1 | 224 | 230 | PF00069 | 0.768 |
MOD_CK2_1 | 521 | 527 | PF00069 | 0.795 |
MOD_CK2_1 | 563 | 569 | PF00069 | 0.675 |
MOD_CMANNOS | 35 | 38 | PF00535 | 0.528 |
MOD_Cter_Amidation | 613 | 616 | PF01082 | 0.670 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.749 |
MOD_GlcNHglycan | 106 | 109 | PF01048 | 0.643 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.689 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.628 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.838 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.779 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.765 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.614 |
MOD_GlcNHglycan | 371 | 374 | PF01048 | 0.569 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.394 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.411 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.411 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.748 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.625 |
MOD_GlcNHglycan | 58 | 62 | PF01048 | 0.617 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.583 |
MOD_GlcNHglycan | 697 | 700 | PF01048 | 0.527 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.743 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.600 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.799 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.787 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.597 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.512 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.347 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.523 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.431 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.760 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.539 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.748 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.604 |
MOD_GSK3_1 | 691 | 698 | PF00069 | 0.639 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.693 |
MOD_N-GLC_1 | 477 | 482 | PF02516 | 0.411 |
MOD_N-GLC_1 | 563 | 568 | PF02516 | 0.581 |
MOD_N-GLC_1 | 618 | 623 | PF02516 | 0.536 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.589 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.641 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.488 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.512 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.282 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.525 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.774 |
MOD_NEK2_1 | 691 | 696 | PF00069 | 0.608 |
MOD_NEK2_2 | 231 | 236 | PF00069 | 0.740 |
MOD_NEK2_2 | 366 | 371 | PF00069 | 0.527 |
MOD_NEK2_2 | 393 | 398 | PF00069 | 0.394 |
MOD_NEK2_2 | 415 | 420 | PF00069 | 0.557 |
MOD_PIKK_1 | 511 | 517 | PF00454 | 0.596 |
MOD_PIKK_1 | 573 | 579 | PF00454 | 0.632 |
MOD_PK_1 | 53 | 59 | PF00069 | 0.534 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.735 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.627 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.743 |
MOD_PKA_2 | 415 | 421 | PF00069 | 0.508 |
MOD_PKB_1 | 475 | 483 | PF00069 | 0.512 |
MOD_PKB_1 | 544 | 552 | PF00069 | 0.719 |
MOD_PKB_1 | 650 | 658 | PF00069 | 0.674 |
MOD_PKB_1 | 706 | 714 | PF00069 | 0.549 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.616 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.562 |
MOD_Plk_2-3 | 123 | 129 | PF00069 | 0.685 |
MOD_Plk_2-3 | 251 | 257 | PF00069 | 0.851 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.685 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.693 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.652 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.592 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.616 |
MOD_Plk_4 | 550 | 556 | PF00069 | 0.752 |
MOD_ProDKin_1 | 280 | 286 | PF00069 | 0.781 |
MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.613 |
MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.768 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.714 |
MOD_ProDKin_1 | 343 | 349 | PF00069 | 0.744 |
MOD_ProDKin_1 | 503 | 509 | PF00069 | 0.755 |
MOD_ProDKin_1 | 535 | 541 | PF00069 | 0.737 |
MOD_ProDKin_1 | 619 | 625 | PF00069 | 0.583 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.554 |
MOD_ProDKin_1 | 87 | 93 | PF00069 | 0.645 |
MOD_SUMO_rev_2 | 83 | 88 | PF00179 | 0.697 |
TRG_DiLeu_BaEn_1 | 488 | 493 | PF01217 | 0.524 |
TRG_DiLeu_BaEn_1 | 731 | 736 | PF01217 | 0.568 |
TRG_DiLeu_BaEn_4 | 163 | 169 | PF01217 | 0.614 |
TRG_DiLeu_BaLyEn_6 | 17 | 22 | PF01217 | 0.607 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 402 | 405 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.581 |
TRG_ENDOCYTIC_2 | 434 | 437 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.632 |
TRG_ENDOCYTIC_2 | 672 | 675 | PF00928 | 0.538 |
TRG_ER_diArg_1 | 450 | 453 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 544 | 547 | PF00400 | 0.727 |
TRG_ER_diArg_1 | 597 | 600 | PF00400 | 0.609 |
TRG_ER_diArg_1 | 647 | 650 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 651 | 653 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 707 | 710 | PF00400 | 0.547 |
TRG_Pf-PMV_PEXEL_1 | 580 | 584 | PF00026 | 0.556 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2L0 | Leptomonas seymouri | 44% | 87% |
A0A3S5H4V1 | Leishmania donovani | 89% | 99% |
A4H369 | Leishmania braziliensis | 70% | 100% |
A4HRG6 | Leishmania infantum | 90% | 100% |
E9AJD0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 99% |