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:0005789 | endoplasmic reticulum membrane | 4 | 2 |
GO:0016020 | membrane | 2 | 2 |
GO:0031090 | organelle membrane | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QGH8
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 2 |
GO:0006458 | 'de novo' protein folding | 3 | 2 |
GO:0006508 | proteolysis | 4 | 2 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010033 | response to organic substance | 3 | 2 |
GO:0010243 | response to organonitrogen compound | 4 | 2 |
GO:0010498 | proteasomal protein catabolic process | 5 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 2 |
GO:0030163 | protein catabolic process | 4 | 2 |
GO:0030433 | ubiquitin-dependent ERAD pathway | 6 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034976 | response to endoplasmic reticulum stress | 4 | 2 |
GO:0035966 | response to topologically incorrect protein | 3 | 2 |
GO:0035967 | cellular response to topologically incorrect protein | 4 | 2 |
GO:0036503 | ERAD pathway | 5 | 2 |
GO:0042221 | response to chemical | 2 | 2 |
GO:0043161 | proteasome-mediated ubiquitin-dependent protein catabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051084 | 'de novo' post-translational protein folding | 4 | 2 |
GO:0051085 | chaperone cofactor-dependent protein refolding | 4 | 2 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0051788 | response to misfolded protein | 4 | 2 |
GO:0061077 | chaperone-mediated protein folding | 3 | 2 |
GO:0070887 | cellular response to chemical stimulus | 3 | 2 |
GO:0071218 | cellular response to misfolded protein | 5 | 2 |
GO:0071310 | cellular response to organic substance | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:1901698 | response to nitrogen compound | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0030544 | Hsp70 protein binding | 4 | 2 |
GO:0031072 | heat shock protein binding | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 501 | 505 | PF00656 | 0.621 |
CLV_C14_Caspase3-7 | 510 | 514 | PF00656 | 0.594 |
CLV_C14_Caspase3-7 | 727 | 731 | PF00656 | 0.573 |
CLV_NRD_NRD_1 | 109 | 111 | PF00675 | 0.412 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 216 | 218 | PF00675 | 0.672 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 393 | 395 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.476 |
CLV_PCSK_FUR_1 | 257 | 261 | PF00082 | 0.488 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.323 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 393 | 395 | PF00082 | 0.632 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.467 |
CLV_Separin_Metazoa | 718 | 722 | PF03568 | 0.528 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.430 |
DEG_SPOP_SBC_1 | 679 | 683 | PF00917 | 0.613 |
DOC_CDC14_PxL_1 | 1 | 9 | PF14671 | 0.419 |
DOC_CKS1_1 | 21 | 26 | PF01111 | 0.437 |
DOC_CYCLIN_RxL_1 | 105 | 118 | PF00134 | 0.293 |
DOC_CYCLIN_RxL_1 | 88 | 96 | PF00134 | 0.287 |
DOC_CYCLIN_yCln2_LP_2 | 50 | 56 | PF00134 | 0.485 |
DOC_MAPK_gen_1 | 105 | 115 | PF00069 | 0.332 |
DOC_MAPK_gen_1 | 383 | 391 | PF00069 | 0.492 |
DOC_PP1_RVXF_1 | 109 | 116 | PF00149 | 0.239 |
DOC_PP2B_LxvP_1 | 19 | 22 | PF13499 | 0.444 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.611 |
DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.597 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 31 | 35 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.439 |
DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 706 | 710 | PF00917 | 0.622 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.589 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 631 | 636 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 671 | 676 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 709 | 714 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.408 |
LIG_14-3-3_CanoR_1 | 265 | 273 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 304 | 310 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 411 | 420 | PF00244 | 0.807 |
LIG_14-3-3_CanoR_1 | 702 | 706 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 721 | 726 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 88 | 94 | PF00244 | 0.356 |
LIG_AP2alpha_2 | 542 | 544 | PF02296 | 0.606 |
LIG_BRCT_BRCA1_1 | 292 | 296 | PF00533 | 0.627 |
LIG_eIF4E_1 | 108 | 114 | PF01652 | 0.305 |
LIG_eIF4E_1 | 385 | 391 | PF01652 | 0.438 |
LIG_EVH1_2 | 13 | 17 | PF00568 | 0.420 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.445 |
LIG_FHA_1 | 235 | 241 | PF00498 | 0.631 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.465 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.625 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.527 |
LIG_FHA_1 | 613 | 619 | PF00498 | 0.408 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.371 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.556 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.691 |
LIG_FHA_2 | 713 | 719 | PF00498 | 0.535 |
LIG_FHA_2 | 725 | 731 | PF00498 | 0.481 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.401 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.342 |
LIG_Integrin_RGD_1 | 561 | 563 | PF01839 | 0.592 |
LIG_LIR_Apic_2 | 272 | 276 | PF02991 | 0.599 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.265 |
LIG_LIR_Nem_3 | 293 | 299 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 714 | 720 | PF02991 | 0.563 |
LIG_LIR_Nem_3 | 87 | 93 | PF02991 | 0.349 |
LIG_PROFILIN_1 | 278 | 284 | PF00235 | 0.534 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.351 |
LIG_SH2_SRC | 134 | 137 | PF00017 | 0.371 |
LIG_SH2_SRC | 717 | 720 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.305 |
LIG_SH2_STAP1 | 628 | 632 | PF00017 | 0.511 |
LIG_SH2_STAT3 | 363 | 366 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.667 |
LIG_SH2_STAT5 | 602 | 605 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 642 | 645 | PF00017 | 0.494 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.612 |
LIG_SH3_3 | 182 | 188 | PF00018 | 0.642 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.550 |
LIG_SH3_3 | 281 | 287 | PF00018 | 0.600 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.497 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.445 |
LIG_TRAF2_1 | 197 | 200 | PF00917 | 0.733 |
LIG_TRAF2_1 | 344 | 347 | PF00917 | 0.607 |
LIG_TYR_ITSM | 713 | 720 | PF00017 | 0.532 |
LIG_WRC_WIRS_1 | 296 | 301 | PF05994 | 0.531 |
LIG_WW_2 | 281 | 284 | PF00397 | 0.551 |
MOD_CDK_SPK_2 | 631 | 636 | PF00069 | 0.556 |
MOD_CDK_SPxxK_3 | 20 | 27 | PF00069 | 0.441 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.622 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.492 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.562 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.657 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.609 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.668 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.716 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.641 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.473 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.576 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.726 |
MOD_CK1_1 | 458 | 464 | PF00069 | 0.544 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.496 |
MOD_CK1_1 | 657 | 663 | PF00069 | 0.636 |
MOD_CK1_1 | 678 | 684 | PF00069 | 0.574 |
MOD_CK1_1 | 704 | 710 | PF00069 | 0.648 |
MOD_CK1_1 | 712 | 718 | PF00069 | 0.514 |
MOD_CK1_1 | 724 | 730 | PF00069 | 0.587 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.648 |
MOD_CK2_1 | 332 | 338 | PF00069 | 0.739 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.650 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.449 |
MOD_CK2_1 | 594 | 600 | PF00069 | 0.466 |
MOD_CK2_1 | 603 | 609 | PF00069 | 0.438 |
MOD_CK2_1 | 646 | 652 | PF00069 | 0.486 |
MOD_CK2_1 | 681 | 687 | PF00069 | 0.791 |
MOD_CK2_1 | 712 | 718 | PF00069 | 0.552 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.413 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.733 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.720 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.597 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.567 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.563 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.659 |
MOD_GlcNHglycan | 504 | 508 | PF01048 | 0.796 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.506 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.562 |
MOD_GlcNHglycan | 548 | 551 | PF01048 | 0.552 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.628 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.511 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.506 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.534 |
MOD_GlcNHglycan | 677 | 680 | PF01048 | 0.585 |
MOD_GlcNHglycan | 694 | 697 | PF01048 | 0.669 |
MOD_GlcNHglycan | 708 | 711 | PF01048 | 0.564 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.647 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.814 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.581 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.593 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.611 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.596 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.623 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.641 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.666 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.548 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.500 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.516 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.744 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.695 |
MOD_GSK3_1 | 701 | 708 | PF00069 | 0.564 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.381 |
MOD_N-GLC_1 | 240 | 245 | PF02516 | 0.572 |
MOD_N-GLC_1 | 429 | 434 | PF02516 | 0.608 |
MOD_N-GLC_2 | 244 | 246 | PF02516 | 0.601 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.500 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.638 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.655 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.533 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.757 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.681 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.535 |
MOD_NEK2_1 | 643 | 648 | PF00069 | 0.543 |
MOD_NEK2_1 | 705 | 710 | PF00069 | 0.736 |
MOD_OFUCOSY | 29 | 35 | PF10250 | 0.460 |
MOD_PIKK_1 | 245 | 251 | PF00454 | 0.492 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.579 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.549 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.612 |
MOD_PIKK_1 | 468 | 474 | PF00454 | 0.425 |
MOD_PIKK_1 | 612 | 618 | PF00454 | 0.404 |
MOD_PIKK_1 | 79 | 85 | PF00454 | 0.375 |
MOD_PK_1 | 721 | 727 | PF00069 | 0.552 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.679 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.487 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.586 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.495 |
MOD_PKA_2 | 534 | 540 | PF00069 | 0.592 |
MOD_PKA_2 | 621 | 627 | PF00069 | 0.613 |
MOD_PKA_2 | 701 | 707 | PF00069 | 0.598 |
MOD_PKB_1 | 322 | 330 | PF00069 | 0.585 |
MOD_PKB_1 | 409 | 417 | PF00069 | 0.571 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.551 |
MOD_Plk_1 | 483 | 489 | PF00069 | 0.517 |
MOD_Plk_2-3 | 338 | 344 | PF00069 | 0.703 |
MOD_Plk_2-3 | 553 | 559 | PF00069 | 0.585 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.524 |
MOD_Plk_4 | 712 | 718 | PF00069 | 0.555 |
MOD_Plk_4 | 721 | 727 | PF00069 | 0.522 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.575 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.586 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.446 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.633 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.596 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.494 |
MOD_ProDKin_1 | 584 | 590 | PF00069 | 0.615 |
MOD_ProDKin_1 | 631 | 637 | PF00069 | 0.555 |
MOD_ProDKin_1 | 671 | 677 | PF00069 | 0.701 |
MOD_ProDKin_1 | 709 | 715 | PF00069 | 0.621 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.402 |
MOD_SUMO_for_1 | 344 | 347 | PF00179 | 0.607 |
MOD_SUMO_rev_2 | 101 | 107 | PF00179 | 0.338 |
TRG_DiLeu_BaLyEn_6 | 572 | 577 | PF01217 | 0.510 |
TRG_ENDOCYTIC_2 | 717 | 720 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.355 |
TRG_ER_diArg_1 | 108 | 110 | PF00400 | 0.325 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.331 |
TRG_ER_diArg_1 | 258 | 260 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 322 | 325 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 393 | 395 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 582 | 585 | PF00400 | 0.589 |
TRG_Pf-PMV_PEXEL_1 | 91 | 96 | PF00026 | 0.331 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC79 | Leptomonas seymouri | 37% | 100% |
A0A3S7WS81 | Leishmania donovani | 83% | 100% |
A4H6Z1 | Leishmania braziliensis | 60% | 100% |
E9AGH2 | Leishmania infantum | 83% | 100% |
E9AP11 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |