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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005773 | vacuole | 5 | 1 |
GO:0005776 | autophagosome | 6 | 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 | 1 |
Related structures:
AlphaFold database: A4HZ84
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 6 |
GO:0006793 | phosphorus metabolic process | 3 | 6 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0006914 | autophagy | 3 | 5 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009056 | catabolic process | 2 | 5 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016310 | phosphorylation | 5 | 6 |
GO:0019538 | protein metabolic process | 3 | 6 |
GO:0036211 | protein modification process | 4 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043412 | macromolecule modification | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044248 | cellular catabolic process | 3 | 5 |
GO:0061919 | process utilizing autophagic mechanism | 2 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007033 | vacuole organization | 5 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 1 |
GO:0046777 | protein autophosphorylation | 6 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1905037 | autophagosome organization | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 6 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004672 | protein kinase activity | 3 | 6 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 6 |
GO:0005488 | binding | 1 | 6 |
GO:0005524 | ATP binding | 5 | 6 |
GO:0016301 | kinase activity | 4 | 6 |
GO:0016740 | transferase activity | 2 | 6 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 6 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 6 |
GO:0017076 | purine nucleotide binding | 4 | 6 |
GO:0030554 | adenyl nucleotide binding | 5 | 6 |
GO:0032553 | ribonucleotide binding | 3 | 6 |
GO:0032555 | purine ribonucleotide binding | 4 | 6 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 6 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 6 |
GO:0036094 | small molecule binding | 2 | 6 |
GO:0043167 | ion binding | 2 | 6 |
GO:0043168 | anion binding | 3 | 6 |
GO:0097159 | organic cyclic compound binding | 2 | 6 |
GO:0097367 | carbohydrate derivative binding | 2 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
GO:1901265 | nucleoside phosphate binding | 3 | 6 |
GO:1901363 | heterocyclic compound binding | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 604 | 608 | PF00656 | 0.589 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.407 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.407 |
CLV_PCSK_PC1ET2_1 | 214 | 216 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.371 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.696 |
CLV_PCSK_SKI1_1 | 610 | 614 | PF00082 | 0.516 |
CLV_Separin_Metazoa | 324 | 328 | PF03568 | 0.407 |
CLV_Separin_Metazoa | 342 | 346 | PF03568 | 0.407 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.838 |
DEG_SCF_FBW7_2 | 60 | 67 | PF00400 | 0.773 |
DEG_SPOP_SBC_1 | 157 | 161 | PF00917 | 0.421 |
DEG_SPOP_SBC_1 | 489 | 493 | PF00917 | 0.827 |
DEG_SPOP_SBC_1 | 561 | 565 | PF00917 | 0.748 |
DEG_SPOP_SBC_1 | 738 | 742 | PF00917 | 0.655 |
DEG_SPOP_SBC_1 | 94 | 98 | PF00917 | 0.804 |
DOC_CKS1_1 | 293 | 298 | PF01111 | 0.407 |
DOC_CKS1_1 | 61 | 66 | PF01111 | 0.780 |
DOC_CYCLIN_RxL_1 | 607 | 616 | PF00134 | 0.509 |
DOC_MAPK_DCC_7 | 392 | 402 | PF00069 | 0.657 |
DOC_MAPK_gen_1 | 166 | 174 | PF00069 | 0.415 |
DOC_MAPK_gen_1 | 221 | 230 | PF00069 | 0.407 |
DOC_MAPK_JIP1_4 | 224 | 230 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 166 | 174 | PF00069 | 0.407 |
DOC_PP2B_LxvP_1 | 139 | 142 | PF13499 | 0.504 |
DOC_PP2B_LxvP_1 | 775 | 778 | PF13499 | 0.801 |
DOC_PP4_FxxP_1 | 402 | 405 | PF00568 | 0.581 |
DOC_PP4_FxxP_1 | 575 | 578 | PF00568 | 0.754 |
DOC_PP4_FxxP_1 | 99 | 102 | PF00568 | 0.815 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.350 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.828 |
DOC_USP7_MATH_1 | 509 | 513 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 521 | 525 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 589 | 593 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 645 | 649 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 738 | 742 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 750 | 754 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.746 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 423 | 428 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 557 | 562 | PF00397 | 0.809 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.679 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 368 | 374 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 377 | 381 | PF00244 | 0.315 |
LIG_14-3-3_CanoR_1 | 385 | 389 | PF00244 | 0.265 |
LIG_14-3-3_CanoR_1 | 610 | 615 | PF00244 | 0.510 |
LIG_APCC_ABBAyCdc20_2 | 216 | 222 | PF00400 | 0.407 |
LIG_BRCT_BRCA1_1 | 167 | 171 | PF00533 | 0.504 |
LIG_BRCT_BRCA1_1 | 285 | 289 | PF00533 | 0.407 |
LIG_BRCT_BRCA1_1 | 95 | 99 | PF00533 | 0.807 |
LIG_EVH1_2 | 398 | 402 | PF00568 | 0.552 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.407 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.370 |
LIG_FHA_1 | 399 | 405 | PF00498 | 0.625 |
LIG_FHA_1 | 561 | 567 | PF00498 | 0.801 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.583 |
LIG_FHA_1 | 681 | 687 | PF00498 | 0.526 |
LIG_FHA_2 | 229 | 235 | PF00498 | 0.504 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.467 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.407 |
LIG_FHA_2 | 705 | 711 | PF00498 | 0.644 |
LIG_FHA_2 | 738 | 744 | PF00498 | 0.760 |
LIG_GBD_Chelix_1 | 614 | 622 | PF00786 | 0.600 |
LIG_LIR_Apic_2 | 295 | 301 | PF02991 | 0.407 |
LIG_LIR_Apic_2 | 401 | 405 | PF02991 | 0.575 |
LIG_LIR_Apic_2 | 573 | 578 | PF02991 | 0.778 |
LIG_LIR_Apic_2 | 96 | 102 | PF02991 | 0.811 |
LIG_LIR_Gen_1 | 133 | 142 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 168 | 177 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 524 | 533 | PF02991 | 0.767 |
LIG_LIR_Gen_1 | 592 | 601 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 133 | 138 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 283 | 288 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 346 | 351 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 524 | 529 | PF02991 | 0.783 |
LIG_LIR_Nem_3 | 592 | 596 | PF02991 | 0.634 |
LIG_MAD2 | 217 | 225 | PF02301 | 0.407 |
LIG_MYND_1 | 395 | 399 | PF01753 | 0.653 |
LIG_PDZ_Class_2 | 784 | 789 | PF00595 | 0.499 |
LIG_Pex14_2 | 285 | 289 | PF04695 | 0.504 |
LIG_PTB_Apo_2 | 540 | 547 | PF02174 | 0.614 |
LIG_PTB_Phospho_1 | 540 | 546 | PF10480 | 0.612 |
LIG_Rb_pABgroove_1 | 112 | 120 | PF01858 | 0.504 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.493 |
LIG_SH2_CRK | 546 | 550 | PF00017 | 0.703 |
LIG_SH2_NCK_1 | 24 | 28 | PF00017 | 0.489 |
LIG_SH2_PTP2 | 13 | 16 | PF00017 | 0.664 |
LIG_SH2_SRC | 598 | 601 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.504 |
LIG_SH2_STAP1 | 626 | 630 | PF00017 | 0.623 |
LIG_SH2_STAP1 | 682 | 686 | PF00017 | 0.518 |
LIG_SH2_STAT3 | 600 | 603 | PF00017 | 0.557 |
LIG_SH2_STAT5 | 13 | 16 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.711 |
LIG_SH2_STAT5 | 598 | 601 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 617 | 620 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 629 | 632 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 682 | 685 | PF00017 | 0.472 |
LIG_SH3_1 | 392 | 398 | PF00018 | 0.659 |
LIG_SH3_1 | 546 | 552 | PF00018 | 0.802 |
LIG_SH3_2 | 464 | 469 | PF14604 | 0.759 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.504 |
LIG_SH3_3 | 390 | 396 | PF00018 | 0.666 |
LIG_SH3_3 | 449 | 455 | PF00018 | 0.830 |
LIG_SH3_3 | 461 | 467 | PF00018 | 0.685 |
LIG_SH3_3 | 481 | 487 | PF00018 | 0.810 |
LIG_SH3_3 | 505 | 511 | PF00018 | 0.791 |
LIG_SH3_3 | 546 | 552 | PF00018 | 0.689 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.675 |
LIG_SH3_3 | 724 | 730 | PF00018 | 0.815 |
LIG_SH3_3 | 775 | 781 | PF00018 | 0.792 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.737 |
LIG_Sin3_3 | 226 | 233 | PF02671 | 0.504 |
LIG_SUMO_SIM_anti_2 | 112 | 119 | PF11976 | 0.407 |
LIG_SUMO_SIM_anti_2 | 592 | 598 | PF11976 | 0.629 |
LIG_SUMO_SIM_par_1 | 319 | 324 | PF11976 | 0.407 |
LIG_TRAF2_1 | 726 | 729 | PF00917 | 0.689 |
LIG_TRFH_1 | 575 | 579 | PF08558 | 0.755 |
LIG_TYR_ITIM | 37 | 42 | PF00017 | 0.581 |
LIG_TYR_ITIM | 596 | 601 | PF00017 | 0.631 |
LIG_UBA3_1 | 210 | 214 | PF00899 | 0.504 |
LIG_WRC_WIRS_1 | 590 | 595 | PF05994 | 0.642 |
LIG_WW_2 | 395 | 398 | PF00397 | 0.644 |
LIG_WW_3 | 140 | 144 | PF00397 | 0.504 |
MOD_CDC14_SPxK_1 | 300 | 303 | PF00782 | 0.407 |
MOD_CDK_SPxK_1 | 297 | 303 | PF00069 | 0.407 |
MOD_CK1_1 | 158 | 164 | PF00069 | 0.378 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.495 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.810 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.827 |
MOD_CK1_1 | 560 | 566 | PF00069 | 0.722 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.517 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.647 |
MOD_CK1_1 | 705 | 711 | PF00069 | 0.732 |
MOD_CK1_1 | 736 | 742 | PF00069 | 0.720 |
MOD_CK1_1 | 753 | 759 | PF00069 | 0.640 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.808 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.504 |
MOD_CK2_1 | 267 | 273 | PF00069 | 0.467 |
MOD_CK2_1 | 480 | 486 | PF00069 | 0.746 |
MOD_CK2_1 | 705 | 711 | PF00069 | 0.782 |
MOD_CK2_1 | 723 | 729 | PF00069 | 0.660 |
MOD_CK2_1 | 737 | 743 | PF00069 | 0.691 |
MOD_GlcNHglycan | 145 | 149 | PF01048 | 0.511 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.504 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.434 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.407 |
MOD_GlcNHglycan | 433 | 436 | PF01048 | 0.830 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.530 |
MOD_GlcNHglycan | 486 | 490 | PF01048 | 0.675 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.715 |
MOD_GlcNHglycan | 692 | 695 | PF01048 | 0.659 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.804 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.562 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.654 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.769 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.596 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.324 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.444 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.415 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.755 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.753 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.700 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.679 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.586 |
MOD_GSK3_1 | 733 | 740 | PF00069 | 0.654 |
MOD_GSK3_1 | 746 | 753 | PF00069 | 0.649 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.765 |
MOD_N-GLC_2 | 647 | 649 | PF02516 | 0.700 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.352 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.350 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.365 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.382 |
MOD_NEK2_1 | 636 | 641 | PF00069 | 0.660 |
MOD_NEK2_1 | 702 | 707 | PF00069 | 0.630 |
MOD_NEK2_1 | 746 | 751 | PF00069 | 0.701 |
MOD_NEK2_2 | 209 | 214 | PF00069 | 0.407 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.407 |
MOD_PIKK_1 | 433 | 439 | PF00454 | 0.813 |
MOD_PIKK_1 | 499 | 505 | PF00454 | 0.709 |
MOD_PIKK_1 | 67 | 73 | PF00454 | 0.757 |
MOD_PK_1 | 480 | 486 | PF00069 | 0.831 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.407 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.367 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.370 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.318 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.274 |
MOD_PKA_2 | 515 | 521 | PF00069 | 0.817 |
MOD_PKA_2 | 640 | 646 | PF00069 | 0.691 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.504 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.540 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.505 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.642 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.449 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.356 |
MOD_ProDKin_1 | 423 | 429 | PF00069 | 0.748 |
MOD_ProDKin_1 | 557 | 563 | PF00069 | 0.808 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.684 |
MOD_SUMO_for_1 | 333 | 336 | PF00179 | 0.504 |
MOD_SUMO_rev_2 | 77 | 84 | PF00179 | 0.826 |
TRG_DiLeu_BaLyEn_6 | 770 | 775 | PF01217 | 0.815 |
TRG_ENDOCYTIC_2 | 13 | 16 | PF00928 | 0.664 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.575 |
TRG_ENDOCYTIC_2 | 598 | 601 | PF00928 | 0.630 |
TRG_ER_diArg_1 | 215 | 217 | PF00400 | 0.407 |
TRG_ER_diArg_1 | 697 | 700 | PF00400 | 0.588 |
TRG_NLS_MonoCore_2 | 213 | 218 | PF00514 | 0.407 |
TRG_Pf-PMV_PEXEL_1 | 349 | 353 | PF00026 | 0.504 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGM5 | Leptomonas seymouri | 44% | 74% |
A0A3S7WWM5 | Leishmania donovani | 100% | 80% |
E9AV51 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QCD0 | Leishmania major | 93% | 100% |