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: E9AKC6
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 | 225 | 229 | PF00656 | 0.525 |
CLV_C14_Caspase3-7 | 463 | 467 | PF00656 | 0.696 |
CLV_C14_Caspase3-7 | 54 | 58 | PF00656 | 0.388 |
CLV_NRD_NRD_1 | 134 | 136 | PF00675 | 0.388 |
CLV_NRD_NRD_1 | 166 | 168 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 531 | 533 | PF00675 | 0.644 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.424 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 397 | 399 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 532 | 536 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.388 |
DEG_APCC_DBOX_1 | 396 | 404 | PF00400 | 0.693 |
DEG_SCF_FBW7_2 | 366 | 373 | PF00400 | 0.651 |
DEG_SCF_TRCP1_1 | 228 | 233 | PF00400 | 0.540 |
DEG_SPOP_SBC_1 | 207 | 211 | PF00917 | 0.550 |
DEG_SPOP_SBC_1 | 290 | 294 | PF00917 | 0.601 |
DEG_SPOP_SBC_1 | 338 | 342 | PF00917 | 0.556 |
DEG_SPOP_SBC_1 | 431 | 435 | PF00917 | 0.629 |
DEG_SPOP_SBC_1 | 437 | 441 | PF00917 | 0.584 |
DEG_SPOP_SBC_1 | 513 | 517 | PF00917 | 0.540 |
DOC_CKS1_1 | 367 | 372 | PF01111 | 0.567 |
DOC_CYCLIN_yCln2_LP_2 | 249 | 252 | PF00134 | 0.599 |
DOC_MAPK_gen_1 | 166 | 174 | PF00069 | 0.388 |
DOC_MAPK_MEF2A_6 | 166 | 174 | PF00069 | 0.388 |
DOC_PP2B_LxvP_1 | 248 | 251 | PF13499 | 0.638 |
DOC_PP4_FxxP_1 | 190 | 193 | PF00568 | 0.561 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.795 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 476 | 480 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 506 | 510 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.358 |
DOC_USP7_MATH_1 | 513 | 517 | PF00917 | 0.532 |
DOC_USP7_MATH_2 | 251 | 257 | PF00917 | 0.611 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 330 | 335 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 485 | 490 | PF00397 | 0.789 |
DOC_WW_Pin1_4 | 514 | 519 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 563 | 568 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.622 |
LIG_14-3-3_CanoR_1 | 121 | 130 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 166 | 174 | PF00244 | 0.375 |
LIG_14-3-3_CanoR_1 | 179 | 185 | PF00244 | 0.233 |
LIG_14-3-3_CanoR_1 | 349 | 359 | PF00244 | 0.681 |
LIG_14-3-3_CanoR_1 | 410 | 419 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 621 | 626 | PF00244 | 0.604 |
LIG_Actin_WH2_2 | 4 | 21 | PF00022 | 0.588 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.443 |
LIG_BRCT_BRCA1_1 | 185 | 189 | PF00533 | 0.545 |
LIG_BRCT_BRCA1_1 | 535 | 539 | PF00533 | 0.527 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.391 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.704 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.620 |
LIG_FHA_1 | 437 | 443 | PF00498 | 0.672 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.469 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.565 |
LIG_FHA_2 | 308 | 314 | PF00498 | 0.749 |
LIG_LIR_Apic_2 | 187 | 193 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 210 | 221 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 210 | 216 | PF02991 | 0.618 |
LIG_LIR_Nem_3 | 253 | 257 | PF02991 | 0.546 |
LIG_MLH1_MIPbox_1 | 186 | 190 | PF16413 | 0.500 |
LIG_MYND_1 | 247 | 251 | PF01753 | 0.606 |
LIG_PCNA_yPIPBox_3 | 85 | 98 | PF02747 | 0.388 |
LIG_RPA_C_Fungi | 130 | 142 | PF08784 | 0.388 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.542 |
LIG_SH2_SRC | 156 | 159 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 156 | 160 | PF00017 | 0.455 |
LIG_SH2_STAT3 | 590 | 593 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 71 | 74 | PF00017 | 0.388 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.776 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.645 |
LIG_SH3_3 | 600 | 606 | PF00018 | 0.794 |
LIG_SUMO_SIM_par_1 | 47 | 54 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 542 | 549 | PF11976 | 0.524 |
LIG_TRAF2_1 | 155 | 158 | PF00917 | 0.226 |
LIG_TRAF2_1 | 175 | 178 | PF00917 | 0.334 |
LIG_TRAF2_1 | 20 | 23 | PF00917 | 0.573 |
LIG_TRAF2_1 | 240 | 243 | PF00917 | 0.649 |
LIG_TRAF2_1 | 81 | 84 | PF00917 | 0.523 |
LIG_TRAF2_2 | 240 | 245 | PF00917 | 0.649 |
LIG_UBA3_1 | 446 | 451 | PF00899 | 0.528 |
LIG_WW_1 | 251 | 254 | PF00397 | 0.520 |
MOD_CDK_SPK_2 | 485 | 490 | PF00069 | 0.706 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.334 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.388 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.739 |
MOD_CK1_1 | 233 | 239 | PF00069 | 0.603 |
MOD_CK1_1 | 289 | 295 | PF00069 | 0.702 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.674 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.627 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.681 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.747 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.791 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.390 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.699 |
MOD_CK1_1 | 549 | 555 | PF00069 | 0.589 |
MOD_CK1_1 | 565 | 571 | PF00069 | 0.521 |
MOD_CK1_1 | 605 | 611 | PF00069 | 0.649 |
MOD_CK1_1 | 620 | 626 | PF00069 | 0.726 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.245 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.548 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.670 |
MOD_CK2_1 | 542 | 548 | PF00069 | 0.631 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.408 |
MOD_Cter_Amidation | 395 | 398 | PF01082 | 0.695 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.516 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.835 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.667 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.654 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.622 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.601 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.670 |
MOD_GlcNHglycan | 346 | 349 | PF01048 | 0.610 |
MOD_GlcNHglycan | 360 | 363 | PF01048 | 0.666 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.680 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.600 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.748 |
MOD_GlcNHglycan | 496 | 499 | PF01048 | 0.710 |
MOD_GlcNHglycan | 507 | 511 | PF01048 | 0.584 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.756 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.388 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.265 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.671 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.563 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.573 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.699 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.540 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.670 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.642 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.611 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.643 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.590 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.472 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.578 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.661 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.694 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.640 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.561 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.614 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.570 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.679 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.647 |
MOD_GSK3_1 | 604 | 611 | PF00069 | 0.718 |
MOD_GSK3_1 | 616 | 623 | PF00069 | 0.695 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.410 |
MOD_N-GLC_1 | 258 | 263 | PF02516 | 0.581 |
MOD_N-GLC_1 | 408 | 413 | PF02516 | 0.523 |
MOD_N-GLC_1 | 476 | 481 | PF02516 | 0.648 |
MOD_N-GLC_1 | 537 | 542 | PF02516 | 0.645 |
MOD_N-GLC_1 | 546 | 551 | PF02516 | 0.643 |
MOD_N-GLC_1 | 563 | 568 | PF02516 | 0.547 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.388 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.536 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.589 |
MOD_NEK2_1 | 337 | 342 | PF00069 | 0.640 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.532 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.562 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.644 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.621 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.529 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.542 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.598 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.388 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.679 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.663 |
MOD_PIKK_1 | 269 | 275 | PF00454 | 0.699 |
MOD_PIKK_1 | 522 | 528 | PF00454 | 0.640 |
MOD_PIKK_1 | 589 | 595 | PF00454 | 0.671 |
MOD_PKA_1 | 328 | 334 | PF00069 | 0.655 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.388 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.246 |
MOD_PKA_2 | 284 | 290 | PF00069 | 0.706 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.695 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.814 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.603 |
MOD_PKA_2 | 469 | 475 | PF00069 | 0.769 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.697 |
MOD_PKA_2 | 620 | 626 | PF00069 | 0.605 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.334 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.608 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.312 |
MOD_Plk_2-3 | 152 | 158 | PF00069 | 0.388 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.605 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.649 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.643 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.469 |
MOD_ProDKin_1 | 203 | 209 | PF00069 | 0.656 |
MOD_ProDKin_1 | 330 | 336 | PF00069 | 0.561 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.613 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.643 |
MOD_ProDKin_1 | 485 | 491 | PF00069 | 0.786 |
MOD_ProDKin_1 | 514 | 520 | PF00069 | 0.730 |
MOD_ProDKin_1 | 563 | 569 | PF00069 | 0.659 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.685 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.624 |
MOD_SUMO_rev_2 | 78 | 87 | PF00179 | 0.388 |
TRG_DiLeu_BaEn_3 | 157 | 163 | PF01217 | 0.263 |
TRG_DiLeu_BaLyEn_6 | 244 | 249 | PF01217 | 0.644 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.546 |
TRG_ER_diArg_1 | 529 | 532 | PF00400 | 0.630 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S5H5G7 | Leishmania donovani | 83% | 94% |
A4H479 | Leishmania braziliensis | 59% | 100% |
A4HSF4 | Leishmania infantum | 83% | 93% |
Q4QJI1 | Leishmania major | 83% | 100% |