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 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QJI1
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:0009966 | regulation of signal transduction | 4 | 2 |
GO:0009968 | negative regulation of signal transduction | 5 | 2 |
GO:0009987 | cellular process | 1 | 6 |
GO:0010646 | regulation of cell communication | 4 | 2 |
GO:0010648 | negative regulation of cell communication | 5 | 2 |
GO:0016311 | dephosphorylation | 5 | 6 |
GO:0019538 | protein metabolic process | 3 | 6 |
GO:0023051 | regulation of signaling | 3 | 2 |
GO:0023057 | negative regulation of signaling | 4 | 2 |
GO:0036211 | protein modification process | 4 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043408 | regulation of MAPK cascade | 6 | 2 |
GO:0043409 | negative regulation of MAPK cascade | 7 | 2 |
GO:0043412 | macromolecule modification | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
GO:0048523 | negative regulation of cellular process | 4 | 2 |
GO:0048583 | regulation of response to stimulus | 3 | 2 |
GO:0048585 | negative regulation of response to stimulus | 4 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
GO:1902531 | regulation of intracellular signal transduction | 5 | 2 |
GO:1902532 | negative regulation of intracellular signal transduction | 6 | 2 |
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 | 246 | 250 | PF00656 | 0.553 |
CLV_C14_Caspase3-7 | 501 | 505 | PF00656 | 0.755 |
CLV_C14_Caspase3-7 | 538 | 542 | PF00656 | 0.560 |
CLV_C14_Caspase3-7 | 86 | 90 | PF00656 | 0.526 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.845 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.815 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.509 |
CLV_NRD_NRD_1 | 569 | 571 | PF00675 | 0.761 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 305 | 307 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.845 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.712 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.815 |
CLV_PCSK_PC1ET2_1 | 305 | 307 | PF00082 | 0.572 |
CLV_PCSK_PC1ET2_1 | 37 | 39 | PF00082 | 0.712 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 434 | 438 | PF00082 | 0.720 |
DEG_APCC_DBOX_1 | 433 | 441 | PF00400 | 0.815 |
DEG_SCF_FBW7_2 | 403 | 410 | PF00400 | 0.742 |
DEG_SPOP_SBC_1 | 2 | 6 | PF00917 | 0.639 |
DEG_SPOP_SBC_1 | 292 | 296 | PF00917 | 0.768 |
DEG_SPOP_SBC_1 | 376 | 380 | PF00917 | 0.594 |
DEG_SPOP_SBC_1 | 445 | 449 | PF00917 | 0.690 |
DOC_CKS1_1 | 404 | 409 | PF01111 | 0.598 |
DOC_CYCLIN_yClb1_LxF_4 | 190 | 196 | PF00134 | 0.364 |
DOC_MAPK_gen_1 | 199 | 207 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 199 | 207 | PF00069 | 0.526 |
DOC_PP2B_LxvP_1 | 284 | 287 | PF13499 | 0.707 |
DOC_PP4_FxxP_1 | 223 | 226 | PF00568 | 0.661 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.812 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.829 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.752 |
DOC_USP7_MATH_1 | 544 | 548 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 83 | 87 | PF00917 | 0.461 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.775 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 510 | 515 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 523 | 528 | PF00397 | 0.821 |
DOC_WW_Pin1_4 | 552 | 557 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 601 | 606 | PF00397 | 0.768 |
DOC_WW_Pin1_4 | 640 | 645 | PF00397 | 0.841 |
LIG_14-3-3_CanoR_1 | 154 | 163 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 199 | 207 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 212 | 218 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 300 | 309 | PF00244 | 0.794 |
LIG_14-3-3_CanoR_1 | 386 | 396 | PF00244 | 0.796 |
LIG_14-3-3_CanoR_1 | 460 | 469 | PF00244 | 0.706 |
LIG_14-3-3_CanoR_1 | 508 | 514 | PF00244 | 0.562 |
LIG_14-3-3_CanoR_1 | 659 | 664 | PF00244 | 0.720 |
LIG_Actin_WH2_2 | 36 | 53 | PF00022 | 0.711 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.644 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.690 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.441 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.558 |
LIG_FHA_1 | 378 | 384 | PF00498 | 0.733 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.816 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.522 |
LIG_FHA_2 | 346 | 352 | PF00498 | 0.832 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.552 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.648 |
LIG_LIR_Apic_2 | 220 | 226 | PF02991 | 0.640 |
LIG_MLH1_MIPbox_1 | 219 | 223 | PF16413 | 0.607 |
LIG_PCNA_yPIPBox_3 | 118 | 131 | PF02747 | 0.526 |
LIG_RPA_C_Fungi | 163 | 175 | PF08784 | 0.526 |
LIG_SH2_GRB2like | 189 | 192 | PF00017 | 0.246 |
LIG_SH2_SRC | 189 | 192 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 189 | 193 | PF00017 | 0.526 |
LIG_SH2_STAT3 | 628 | 631 | PF00017 | 0.757 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.252 |
LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.501 |
LIG_SH3_2 | 24 | 29 | PF14604 | 0.668 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.704 |
LIG_SH3_3 | 21 | 27 | PF00018 | 0.674 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.811 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.754 |
LIG_SUMO_SIM_par_1 | 282 | 288 | PF11976 | 0.526 |
LIG_SUMO_SIM_par_1 | 79 | 86 | PF11976 | 0.579 |
LIG_TRAF2_1 | 113 | 116 | PF00917 | 0.526 |
LIG_TRAF2_1 | 208 | 211 | PF00917 | 0.433 |
LIG_TRAF2_1 | 275 | 278 | PF00917 | 0.608 |
LIG_TRAF2_1 | 463 | 466 | PF00917 | 0.685 |
LIG_TRAF2_1 | 498 | 501 | PF00917 | 0.798 |
LIG_TRAF2_1 | 52 | 55 | PF00917 | 0.697 |
LIG_TRAF2_2 | 275 | 280 | PF00917 | 0.745 |
LIG_Vh1_VBS_1 | 468 | 486 | PF01044 | 0.542 |
MOD_CDC14_SPxK_1 | 26 | 29 | PF00782 | 0.663 |
MOD_CDK_SPK_2 | 523 | 528 | PF00069 | 0.852 |
MOD_CDK_SPxK_1 | 23 | 29 | PF00069 | 0.670 |
MOD_CK1_1 | 157 | 163 | PF00069 | 0.485 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.526 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.828 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.699 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.746 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.601 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.810 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.613 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.695 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.842 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.825 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.825 |
MOD_CK1_1 | 574 | 580 | PF00069 | 0.813 |
MOD_CK1_1 | 613 | 619 | PF00069 | 0.644 |
MOD_CK1_1 | 658 | 664 | PF00069 | 0.710 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.492 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.758 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.765 |
MOD_CK2_1 | 537 | 543 | PF00069 | 0.794 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.639 |
MOD_CK2_1 | 580 | 586 | PF00069 | 0.759 |
MOD_CK2_1 | 88 | 94 | PF00069 | 0.433 |
MOD_Cter_Amidation | 432 | 435 | PF01082 | 0.814 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.373 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.783 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.572 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.730 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.577 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.766 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.632 |
MOD_GlcNHglycan | 397 | 400 | PF01048 | 0.604 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.835 |
MOD_GlcNHglycan | 534 | 537 | PF01048 | 0.860 |
MOD_GlcNHglycan | 545 | 549 | PF01048 | 0.658 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.779 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.712 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.509 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.526 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.444 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.698 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.800 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.694 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.731 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.713 |
MOD_GSK3_1 | 341 | 348 | PF00069 | 0.656 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.716 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.630 |
MOD_GSK3_1 | 444 | 451 | PF00069 | 0.777 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.736 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.775 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.608 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.765 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.756 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.839 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.778 |
MOD_GSK3_1 | 638 | 645 | PF00069 | 0.645 |
MOD_GSK3_1 | 654 | 661 | PF00069 | 0.710 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.528 |
MOD_N-GLC_1 | 133 | 138 | PF02516 | 0.246 |
MOD_N-GLC_1 | 267 | 272 | PF02516 | 0.719 |
MOD_N-GLC_1 | 514 | 519 | PF02516 | 0.741 |
MOD_N-GLC_1 | 575 | 580 | PF02516 | 0.790 |
MOD_N-GLC_1 | 587 | 592 | PF02516 | 0.722 |
MOD_N-GLC_1 | 601 | 606 | PF02516 | 0.612 |
MOD_N-GLC_2 | 487 | 489 | PF02516 | 0.693 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.516 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.600 |
MOD_NEK2_1 | 375 | 380 | PF00069 | 0.738 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.746 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.464 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.767 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.764 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.845 |
MOD_PIKK_1 | 528 | 534 | PF00454 | 0.572 |
MOD_PIKK_1 | 560 | 566 | PF00454 | 0.752 |
MOD_PIKK_1 | 627 | 633 | PF00454 | 0.849 |
MOD_PIKK_1 | 638 | 644 | PF00454 | 0.664 |
MOD_PK_1 | 320 | 326 | PF00069 | 0.685 |
MOD_PKA_1 | 366 | 372 | PF00069 | 0.743 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.526 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.232 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.699 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.792 |
MOD_PKA_2 | 337 | 343 | PF00069 | 0.761 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.831 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.552 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.756 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.836 |
MOD_PKA_2 | 658 | 664 | PF00069 | 0.721 |
MOD_PKB_1 | 601 | 609 | PF00069 | 0.723 |
MOD_Plk_1 | 157 | 163 | PF00069 | 0.433 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.555 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.741 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.356 |
MOD_Plk_2-3 | 185 | 191 | PF00069 | 0.526 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.677 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.713 |
MOD_Plk_4 | 479 | 485 | PF00069 | 0.725 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.639 |
MOD_Plk_4 | 648 | 654 | PF00069 | 0.688 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.522 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.707 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.774 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.540 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.680 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.728 |
MOD_ProDKin_1 | 510 | 516 | PF00069 | 0.657 |
MOD_ProDKin_1 | 523 | 529 | PF00069 | 0.819 |
MOD_ProDKin_1 | 552 | 558 | PF00069 | 0.743 |
MOD_ProDKin_1 | 601 | 607 | PF00069 | 0.769 |
MOD_ProDKin_1 | 640 | 646 | PF00069 | 0.840 |
MOD_SUMO_rev_2 | 110 | 120 | PF00179 | 0.526 |
TRG_DiLeu_BaEn_1 | 115 | 120 | PF01217 | 0.246 |
TRG_DiLeu_BaEn_4 | 464 | 470 | PF01217 | 0.543 |
TRG_DiLeu_BaLyEn_6 | 279 | 284 | PF01217 | 0.725 |
TRG_ER_diArg_1 | 567 | 570 | PF00400 | 0.748 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H5G7 | Leishmania donovani | 90% | 100% |
A4H479 | Leishmania braziliensis | 57% | 76% |
A4HSF4 | Leishmania infantum | 90% | 99% |
E9AKC6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |