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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H369
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0007264 | small GTPase mediated signal transduction | 4 | 1 |
GO:0007265 | Ras protein signal transduction | 5 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0035556 | intracellular signal transduction | 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:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 7 |
GO:0008270 | zinc ion binding | 6 | 7 |
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:0003824 | catalytic activity | 1 | 2 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 146 | 150 | PF00656 | 0.807 |
CLV_C14_Caspase3-7 | 453 | 457 | PF00656 | 0.750 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.861 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 543 | 545 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 568 | 570 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 607 | 609 | PF00675 | 0.598 |
CLV_PCSK_FUR_1 | 347 | 351 | PF00082 | 0.346 |
CLV_PCSK_FUR_1 | 501 | 505 | PF00082 | 0.581 |
CLV_PCSK_FUR_1 | 540 | 544 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.627 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.642 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 542 | 544 | PF00082 | 0.630 |
CLV_PCSK_PC7_1 | 539 | 545 | PF00082 | 0.630 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 543 | 547 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 569 | 573 | PF00082 | 0.397 |
CLV_Separin_Metazoa | 14 | 18 | PF03568 | 0.577 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.508 |
DEG_SPOP_SBC_1 | 423 | 427 | PF00917 | 0.761 |
DOC_CKS1_1 | 185 | 190 | PF01111 | 0.854 |
DOC_CYCLIN_yCln2_LP_2 | 55 | 61 | PF00134 | 0.741 |
DOC_PP2B_LxvP_1 | 55 | 58 | PF13499 | 0.754 |
DOC_PP4_FxxP_1 | 75 | 78 | PF00568 | 0.544 |
DOC_SPAK_OSR1_1 | 313 | 317 | PF12202 | 0.545 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.826 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 631 | 635 | PF00917 | 0.657 |
DOC_USP7_MATH_2 | 58 | 64 | PF00917 | 0.573 |
DOC_WW_Pin1_4 | 174 | 179 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.774 |
DOC_WW_Pin1_4 | 228 | 233 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 176 | 185 | PF00244 | 0.788 |
LIG_14-3-3_CanoR_1 | 211 | 220 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 313 | 317 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 372 | 382 | PF00244 | 0.599 |
LIG_14-3-3_CanoR_1 | 502 | 511 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 93 | 99 | PF00244 | 0.572 |
LIG_APCC_ABBA_1 | 380 | 385 | PF00400 | 0.620 |
LIG_APCC_ABBAyCdc20_2 | 379 | 385 | PF00400 | 0.546 |
LIG_BIR_III_2 | 64 | 68 | PF00653 | 0.661 |
LIG_BRCT_BRCA1_1 | 268 | 272 | PF00533 | 0.564 |
LIG_BRCT_BRCA1_1 | 377 | 381 | PF00533 | 0.546 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.581 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.542 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.475 |
LIG_FHA_1 | 436 | 442 | PF00498 | 0.559 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.543 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.627 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.675 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.411 |
LIG_FHA_1 | 601 | 607 | PF00498 | 0.664 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.546 |
LIG_FHA_2 | 423 | 429 | PF00498 | 0.651 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.432 |
LIG_LIR_Gen_1 | 11 | 20 | PF02991 | 0.654 |
LIG_LIR_Gen_1 | 120 | 130 | PF02991 | 0.762 |
LIG_LIR_Gen_1 | 297 | 307 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 315 | 323 | PF02991 | 0.387 |
LIG_LIR_Gen_1 | 330 | 339 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 11 | 15 | PF02991 | 0.693 |
LIG_LIR_Nem_3 | 120 | 125 | PF02991 | 0.748 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 297 | 302 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 315 | 320 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 330 | 334 | PF02991 | 0.546 |
LIG_MYND_1 | 195 | 199 | PF01753 | 0.574 |
LIG_PCNA_PIPBox_1 | 581 | 590 | PF02747 | 0.532 |
LIG_PDZ_Class_1 | 630 | 635 | PF00595 | 0.552 |
LIG_SH2_CRK | 28 | 32 | PF00017 | 0.590 |
LIG_SH2_CRK | 299 | 303 | PF00017 | 0.411 |
LIG_SH2_CRK | 317 | 321 | PF00017 | 0.584 |
LIG_SH2_STAP1 | 331 | 335 | PF00017 | 0.546 |
LIG_SH2_STAP1 | 479 | 483 | PF00017 | 0.544 |
LIG_SH2_STAP1 | 494 | 498 | PF00017 | 0.565 |
LIG_SH2_STAT3 | 478 | 481 | PF00017 | 0.650 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.591 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.676 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.730 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.850 |
LIG_SH3_3 | 204 | 210 | PF00018 | 0.589 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.636 |
LIG_SH3_3 | 246 | 252 | PF00018 | 0.597 |
LIG_SUMO_SIM_anti_2 | 11 | 17 | PF11976 | 0.580 |
LIG_SUMO_SIM_anti_2 | 385 | 394 | PF11976 | 0.571 |
LIG_SUMO_SIM_anti_2 | 552 | 559 | PF11976 | 0.653 |
LIG_SUMO_SIM_par_1 | 66 | 71 | PF11976 | 0.675 |
LIG_TRAF2_1 | 46 | 49 | PF00917 | 0.614 |
LIG_TRAF2_1 | 470 | 473 | PF00917 | 0.577 |
LIG_TRAF2_1 | 618 | 621 | PF00917 | 0.603 |
LIG_WW_3 | 208 | 212 | PF00397 | 0.547 |
MOD_CDK_SPxxK_3 | 195 | 202 | PF00069 | 0.707 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.786 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.690 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.546 |
MOD_CK1_1 | 427 | 433 | PF00069 | 0.555 |
MOD_CK1_1 | 524 | 530 | PF00069 | 0.567 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.368 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.765 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.468 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.766 |
MOD_CK2_1 | 467 | 473 | PF00069 | 0.681 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.629 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.566 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.844 |
MOD_GlcNHglycan | 182 | 185 | PF01048 | 0.783 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.636 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.411 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.346 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.740 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.625 |
MOD_GlcNHglycan | 515 | 518 | PF01048 | 0.593 |
MOD_GlcNHglycan | 589 | 592 | PF01048 | 0.520 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.552 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.745 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.795 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.692 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.512 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.533 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.409 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.777 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.639 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.556 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.588 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.599 |
MOD_GSK3_1 | 583 | 590 | PF00069 | 0.633 |
MOD_N-GLC_1 | 374 | 379 | PF02516 | 0.346 |
MOD_N-GLC_1 | 428 | 433 | PF02516 | 0.557 |
MOD_N-GLC_1 | 467 | 472 | PF02516 | 0.586 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.512 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.282 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.620 |
MOD_NEK2_1 | 450 | 455 | PF00069 | 0.595 |
MOD_NEK2_1 | 526 | 531 | PF00069 | 0.505 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.635 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.602 |
MOD_NEK2_2 | 124 | 129 | PF00069 | 0.723 |
MOD_NEK2_2 | 312 | 317 | PF00069 | 0.542 |
MOD_PIKK_1 | 186 | 192 | PF00454 | 0.626 |
MOD_PIKK_1 | 477 | 483 | PF00454 | 0.644 |
MOD_PIKK_1 | 600 | 606 | PF00454 | 0.531 |
MOD_PIKK_1 | 611 | 617 | PF00454 | 0.421 |
MOD_PKA_1 | 503 | 509 | PF00069 | 0.424 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.634 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.493 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.448 |
MOD_PKA_2 | 373 | 379 | PF00069 | 0.448 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.635 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.566 |
MOD_PKB_1 | 372 | 380 | PF00069 | 0.618 |
MOD_PKB_1 | 501 | 509 | PF00069 | 0.423 |
MOD_PKB_1 | 542 | 550 | PF00069 | 0.720 |
MOD_Plk_1 | 522 | 528 | PF00069 | 0.486 |
MOD_Plk_2-3 | 145 | 151 | PF00069 | 0.831 |
MOD_Plk_2-3 | 8 | 14 | PF00069 | 0.720 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.690 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.636 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.521 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.740 |
MOD_Plk_4 | 8 | 14 | PF00069 | 0.720 |
MOD_ProDKin_1 | 174 | 180 | PF00069 | 0.792 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.640 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.776 |
MOD_ProDKin_1 | 228 | 234 | PF00069 | 0.688 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.644 |
MOD_SUMO_rev_2 | 489 | 499 | PF00179 | 0.426 |
TRG_DiLeu_BaEn_1 | 385 | 390 | PF01217 | 0.533 |
TRG_DiLeu_BaEn_4 | 48 | 54 | PF01217 | 0.631 |
TRG_DiLeu_BaLyEn_6 | 263 | 268 | PF01217 | 0.597 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.591 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 317 | 320 | PF00928 | 0.586 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.642 |
TRG_ENDOCYTIC_2 | 564 | 567 | PF00928 | 0.551 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 501 | 504 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 539 | 542 | PF00400 | 0.629 |
TRG_ER_diArg_1 | 543 | 545 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 599 | 602 | PF00400 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 544 | 548 | PF00026 | 0.591 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2L0 | Leptomonas seymouri | 42% | 75% |
A0A3S5H4V1 | Leishmania donovani | 71% | 85% |
A4HRG6 | Leishmania infantum | 71% | 85% |
E9AC34 | Leishmania major | 70% | 100% |
E9AJD0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 85% |