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:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HSF4
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 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:0008152 | metabolic process | 1 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016311 | dephosphorylation | 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:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
GO:0009966 | regulation of signal transduction | 4 | 1 |
GO:0009968 | negative regulation of signal transduction | 5 | 1 |
GO:0010646 | regulation of cell communication | 4 | 1 |
GO:0010648 | negative regulation of cell communication | 5 | 1 |
GO:0023051 | regulation of signaling | 3 | 1 |
GO:0023057 | negative regulation of signaling | 4 | 1 |
GO:0043408 | regulation of MAPK cascade | 6 | 1 |
GO:0043409 | negative regulation of MAPK cascade | 7 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0048583 | regulation of response to stimulus | 3 | 1 |
GO:0048585 | negative regulation of response to stimulus | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 1 |
GO:1902532 | negative regulation of intracellular signal transduction | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 6 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 6 |
GO:0004725 | protein tyrosine phosphatase activity | 4 | 6 |
GO:0008138 | protein tyrosine/serine/threonine phosphatase activity | 4 | 6 |
GO:0016787 | hydrolase activity | 2 | 6 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 6 |
GO:0016791 | phosphatase activity | 5 | 6 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 6 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 507 | 511 | PF00656 | 0.743 |
CLV_C14_Caspase3-7 | 86 | 90 | PF00656 | 0.526 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 371 | 373 | PF00675 | 0.844 |
CLV_NRD_NRD_1 | 440 | 442 | PF00675 | 0.812 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 575 | 577 | PF00675 | 0.759 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.844 |
CLV_PCSK_KEX2_1 | 440 | 442 | PF00082 | 0.812 |
CLV_PCSK_PC1ET2_1 | 37 | 39 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.688 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 576 | 580 | PF00082 | 0.711 |
DEG_APCC_DBOX_1 | 439 | 447 | PF00400 | 0.812 |
DEG_SCF_FBW7_2 | 409 | 416 | PF00400 | 0.746 |
DEG_SPOP_SBC_1 | 2 | 6 | PF00917 | 0.639 |
DEG_SPOP_SBC_1 | 293 | 297 | PF00917 | 0.781 |
DEG_SPOP_SBC_1 | 451 | 455 | PF00917 | 0.663 |
DOC_CYCLIN_yCln2_LP_2 | 285 | 288 | PF00134 | 0.669 |
DOC_MAPK_gen_1 | 199 | 207 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 199 | 207 | PF00069 | 0.526 |
DOC_PP2B_LxvP_1 | 284 | 287 | PF13499 | 0.725 |
DOC_PP4_FxxP_1 | 223 | 226 | PF00568 | 0.656 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.809 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 358 | 362 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.401 |
DOC_USP7_MATH_2 | 287 | 293 | PF00917 | 0.675 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.807 |
DOC_WW_Pin1_4 | 558 | 563 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 607 | 612 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 646 | 651 | PF00397 | 0.825 |
LIG_14-3-3_CanoR_1 | 154 | 163 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 199 | 207 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 212 | 218 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 305 | 312 | PF00244 | 0.786 |
LIG_14-3-3_CanoR_1 | 388 | 394 | PF00244 | 0.713 |
LIG_14-3-3_CanoR_1 | 466 | 475 | PF00244 | 0.713 |
LIG_14-3-3_CanoR_1 | 665 | 670 | PF00244 | 0.712 |
LIG_Actin_WH2_2 | 36 | 53 | PF00022 | 0.697 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.645 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.686 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.433 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.722 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.642 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.818 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.583 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.826 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.611 |
LIG_LIR_Apic_2 | 220 | 226 | PF02991 | 0.634 |
LIG_LYPXL_L_2 | 72 | 81 | PF13949 | 0.420 |
LIG_MLH1_MIPbox_1 | 219 | 223 | PF16413 | 0.601 |
LIG_MYND_1 | 283 | 287 | PF01753 | 0.682 |
LIG_PCNA_yPIPBox_3 | 118 | 131 | PF02747 | 0.526 |
LIG_RPA_C_Fungi | 163 | 175 | PF08784 | 0.526 |
LIG_SH2_SRC | 189 | 192 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 189 | 193 | PF00017 | 0.501 |
LIG_SH2_STAT3 | 634 | 637 | PF00017 | 0.741 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.412 |
LIG_SH3_2 | 24 | 29 | PF14604 | 0.664 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.704 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.668 |
LIG_SH3_3 | 428 | 434 | PF00018 | 0.798 |
LIG_SH3_3 | 530 | 536 | PF00018 | 0.737 |
LIG_SH3_3 | 644 | 650 | PF00018 | 0.780 |
LIG_SUMO_SIM_par_1 | 79 | 86 | PF11976 | 0.578 |
LIG_TRAF2_1 | 113 | 116 | PF00917 | 0.532 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.386 |
LIG_TRAF2_1 | 469 | 472 | PF00917 | 0.700 |
LIG_TRAF2_1 | 504 | 507 | PF00917 | 0.792 |
LIG_TRAF2_1 | 52 | 55 | PF00917 | 0.671 |
LIG_TRAF2_2 | 276 | 281 | PF00917 | 0.740 |
MOD_CDC14_SPxK_1 | 26 | 29 | PF00782 | 0.659 |
MOD_CDK_SPK_2 | 529 | 534 | PF00069 | 0.838 |
MOD_CDK_SPxK_1 | 23 | 29 | PF00069 | 0.665 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.339 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.526 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.711 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.700 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.757 |
MOD_CK1_1 | 300 | 306 | PF00069 | 0.639 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.803 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.604 |
MOD_CK1_1 | 390 | 396 | PF00069 | 0.688 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.840 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.800 |
MOD_CK1_1 | 516 | 522 | PF00069 | 0.815 |
MOD_CK1_1 | 580 | 586 | PF00069 | 0.792 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.700 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.397 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.750 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.790 |
MOD_CK2_1 | 543 | 549 | PF00069 | 0.783 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.594 |
MOD_CK2_1 | 586 | 592 | PF00069 | 0.745 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.353 |
MOD_Cter_Amidation | 438 | 441 | PF01082 | 0.812 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.526 |
MOD_GlcNHglycan | 244 | 247 | PF01048 | 0.767 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.542 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.785 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.724 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.574 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.762 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.623 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.593 |
MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.809 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.611 |
MOD_GlcNHglycan | 518 | 521 | PF01048 | 0.785 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.844 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.767 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.705 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.517 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.526 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.314 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.730 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.816 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.681 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.721 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.657 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.647 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.712 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.613 |
MOD_GSK3_1 | 450 | 457 | PF00069 | 0.751 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.790 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.763 |
MOD_GSK3_1 | 552 | 559 | PF00069 | 0.756 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.743 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.820 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.762 |
MOD_GSK3_1 | 660 | 667 | PF00069 | 0.699 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.546 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.700 |
MOD_N-GLC_1 | 520 | 525 | PF02516 | 0.734 |
MOD_N-GLC_1 | 552 | 557 | PF02516 | 0.713 |
MOD_N-GLC_1 | 581 | 586 | PF02516 | 0.768 |
MOD_N-GLC_1 | 593 | 598 | PF02516 | 0.713 |
MOD_N-GLC_1 | 607 | 612 | PF02516 | 0.594 |
MOD_N-GLC_2 | 493 | 495 | PF02516 | 0.699 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.526 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.614 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.718 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.749 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.730 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.722 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.526 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.699 |
MOD_PIKK_1 | 269 | 275 | PF00454 | 0.748 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.828 |
MOD_PIKK_1 | 566 | 572 | PF00454 | 0.751 |
MOD_PIKK_1 | 633 | 639 | PF00454 | 0.835 |
MOD_PK_1 | 325 | 331 | PF00069 | 0.673 |
MOD_PKA_1 | 371 | 377 | PF00069 | 0.742 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.454 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.314 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.700 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.782 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.755 |
MOD_PKA_2 | 371 | 377 | PF00069 | 0.831 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.542 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.747 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.738 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.820 |
MOD_PKA_2 | 664 | 670 | PF00069 | 0.712 |
MOD_PKB_1 | 607 | 615 | PF00069 | 0.704 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.377 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.692 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.554 |
MOD_Plk_2-3 | 185 | 191 | PF00069 | 0.526 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.599 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.701 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.731 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.594 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.685 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.444 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.703 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.754 |
MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.685 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.686 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.733 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.804 |
MOD_ProDKin_1 | 558 | 564 | PF00069 | 0.737 |
MOD_ProDKin_1 | 607 | 613 | PF00069 | 0.749 |
MOD_ProDKin_1 | 646 | 652 | PF00069 | 0.827 |
MOD_SUMO_rev_2 | 110 | 120 | PF00179 | 0.526 |
TRG_DiLeu_BaLyEn_6 | 280 | 285 | PF01217 | 0.740 |
TRG_ER_diArg_1 | 573 | 576 | PF00400 | 0.750 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H5G7 | Leishmania donovani | 99% | 100% |
A4H479 | Leishmania braziliensis | 59% | 100% |
E9AKC6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 98% |
Q4QJI1 | Leishmania major | 90% | 99% |