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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7XAR2
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016311 | dephosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 12 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 12 |
GO:0016791 | phosphatase activity | 5 | 12 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:0017018 | myosin phosphatase activity | 5 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 296 | 300 | PF00656 | 0.625 |
CLV_C14_Caspase3-7 | 336 | 340 | PF00656 | 0.385 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 143 | 145 | PF00675 | 0.304 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.543 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.385 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 511 | 513 | PF00675 | 0.410 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 360 | 362 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 491 | 493 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 510 | 512 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 189 | 191 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 575 | 577 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 230 | 234 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 517 | 521 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 556 | 560 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.682 |
CLV_Separin_Metazoa | 553 | 557 | PF03568 | 0.613 |
DEG_APCC_DBOX_1 | 12 | 20 | PF00400 | 0.438 |
DEG_APCC_DBOX_1 | 522 | 530 | PF00400 | 0.501 |
DEG_COP1_1 | 461 | 470 | PF00400 | 0.562 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.651 |
DOC_CYCLIN_RxL_1 | 408 | 417 | PF00134 | 0.300 |
DOC_CYCLIN_yCln2_LP_2 | 14 | 20 | PF00134 | 0.442 |
DOC_MAPK_DCC_7 | 13 | 21 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 13 | 21 | PF00069 | 0.451 |
DOC_MAPK_gen_1 | 302 | 310 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 13 | 21 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 302 | 310 | PF00069 | 0.413 |
DOC_MAPK_RevD_3 | 131 | 144 | PF00069 | 0.577 |
DOC_PIKK_1 | 399 | 406 | PF02985 | 0.448 |
DOC_PP1_RVXF_1 | 210 | 217 | PF00149 | 0.419 |
DOC_PP2B_LxvP_1 | 14 | 17 | PF13499 | 0.422 |
DOC_PP2B_LxvP_1 | 416 | 419 | PF13499 | 0.398 |
DOC_PP2B_PxIxI_1 | 16 | 22 | PF00149 | 0.488 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.381 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.763 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.292 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.342 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.410 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.628 |
LIG_14-3-3_CanoR_1 | 144 | 154 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 230 | 240 | PF00244 | 0.687 |
LIG_14-3-3_CanoR_1 | 316 | 324 | PF00244 | 0.417 |
LIG_14-3-3_CanoR_1 | 412 | 417 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 523 | 529 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 59 | 64 | PF00244 | 0.703 |
LIG_Actin_WH2_2 | 303 | 318 | PF00022 | 0.398 |
LIG_APCC_ABBAyCdc20_2 | 143 | 149 | PF00400 | 0.634 |
LIG_BRCT_BRCA1_1 | 279 | 283 | PF00533 | 0.429 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.469 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.437 |
LIG_FHA_2 | 153 | 159 | PF00498 | 0.571 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.398 |
LIG_FHA_2 | 61 | 67 | PF00498 | 0.714 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.525 |
LIG_IBAR_NPY_1 | 341 | 343 | PF08397 | 0.456 |
LIG_LIR_Apic_2 | 471 | 476 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 567 | 577 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 376 | 380 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 567 | 573 | PF02991 | 0.510 |
LIG_Pex14_2 | 430 | 434 | PF04695 | 0.449 |
LIG_PTAP_UEV_1 | 578 | 583 | PF05743 | 0.623 |
LIG_PTB_Apo_2 | 338 | 345 | PF02174 | 0.363 |
LIG_PTB_Phospho_1 | 338 | 344 | PF10480 | 0.385 |
LIG_Rb_LxCxE_1 | 243 | 261 | PF01857 | 0.594 |
LIG_REV1ctd_RIR_1 | 168 | 176 | PF16727 | 0.503 |
LIG_SH2_CRK | 320 | 324 | PF00017 | 0.449 |
LIG_SH2_GRB2like | 343 | 346 | PF00017 | 0.456 |
LIG_SH2_PTP2 | 18 | 21 | PF00017 | 0.500 |
LIG_SH2_SRC | 162 | 165 | PF00017 | 0.510 |
LIG_SH2_SRC | 18 | 21 | PF00017 | 0.298 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 105 | 108 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 480 | 483 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.488 |
LIG_SH3_1 | 125 | 131 | PF00018 | 0.598 |
LIG_SH3_1 | 200 | 206 | PF00018 | 0.651 |
LIG_SH3_1 | 576 | 582 | PF00018 | 0.578 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.571 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.725 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.390 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.535 |
LIG_SH3_3 | 576 | 582 | PF00018 | 0.578 |
LIG_SUMO_SIM_anti_2 | 525 | 530 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 305 | 311 | PF11976 | 0.420 |
LIG_SUMO_SIM_par_1 | 367 | 373 | PF11976 | 0.389 |
LIG_TRAF2_1 | 185 | 188 | PF00917 | 0.605 |
LIG_TRAF2_1 | 205 | 208 | PF00917 | 0.621 |
LIG_TYR_ITIM | 16 | 21 | PF00017 | 0.492 |
LIG_UBA3_1 | 10 | 15 | PF00899 | 0.527 |
LIG_UBA3_1 | 368 | 375 | PF00899 | 0.437 |
LIG_WRC_WIRS_1 | 35 | 40 | PF05994 | 0.417 |
MOD_CDC14_SPxK_1 | 243 | 246 | PF00782 | 0.665 |
MOD_CDC14_SPxK_1 | 313 | 316 | PF00782 | 0.262 |
MOD_CDK_SPxK_1 | 240 | 246 | PF00069 | 0.651 |
MOD_CDK_SPxK_1 | 310 | 316 | PF00069 | 0.262 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.402 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.557 |
MOD_CK1_1 | 463 | 469 | PF00069 | 0.592 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.489 |
MOD_CK2_1 | 182 | 188 | PF00069 | 0.621 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.421 |
MOD_CK2_1 | 399 | 405 | PF00069 | 0.339 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.592 |
MOD_CK2_1 | 91 | 97 | PF00069 | 0.526 |
MOD_Cter_Amidation | 176 | 179 | PF01082 | 0.616 |
MOD_Cter_Amidation | 358 | 361 | PF01082 | 0.475 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.617 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.495 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.430 |
MOD_GlcNHglycan | 207 | 211 | PF01048 | 0.477 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.416 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.668 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.636 |
MOD_GlcNHglycan | 579 | 582 | PF01048 | 0.706 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.333 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.574 |
MOD_GSK3_1 | 214 | 221 | PF00069 | 0.493 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.516 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.401 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.669 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.659 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.434 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.362 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.373 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.581 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.572 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.430 |
MOD_NEK2_2 | 351 | 356 | PF00069 | 0.363 |
MOD_PIKK_1 | 71 | 77 | PF00454 | 0.675 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.398 |
MOD_PKA_2 | 522 | 528 | PF00069 | 0.554 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.449 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.437 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.338 |
MOD_Plk_1 | 436 | 442 | PF00069 | 0.510 |
MOD_Plk_1 | 501 | 507 | PF00069 | 0.477 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.512 |
MOD_Plk_2-3 | 399 | 405 | PF00069 | 0.385 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.368 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.625 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.566 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.507 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.267 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.483 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.752 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.306 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.651 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.510 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.342 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.410 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.634 |
MOD_SUMO_rev_2 | 362 | 369 | PF00179 | 0.384 |
TRG_DiLeu_BaEn_1 | 149 | 154 | PF01217 | 0.582 |
TRG_DiLeu_BaEn_1 | 258 | 263 | PF01217 | 0.613 |
TRG_DiLeu_BaEn_2 | 96 | 102 | PF01217 | 0.512 |
TRG_DiLeu_BaLyEn_6 | 128 | 133 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.455 |
TRG_ER_diArg_1 | 142 | 144 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 178 | 180 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 320 | 322 | PF00400 | 0.381 |
TRG_ER_diArg_1 | 490 | 493 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 509 | 512 | PF00400 | 0.301 |
TRG_NES_CRM1_1 | 404 | 417 | PF08389 | 0.300 |
TRG_Pf-PMV_PEXEL_1 | 121 | 126 | PF00026 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 378 | 383 | PF00026 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 412 | 417 | PF00026 | 0.378 |
TRG_Pf-PMV_PEXEL_1 | 46 | 50 | PF00026 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 492 | 496 | PF00026 | 0.506 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Q6 | Leptomonas seymouri | 61% | 100% |
A0A0S4IM91 | Bodo saltans | 29% | 100% |
A0A0S4IRQ5 | Bodo saltans | 29% | 100% |
A0A1X0P810 | Trypanosomatidae | 44% | 98% |
A4HNY3 | Leishmania braziliensis | 81% | 100% |
A4ICL1 | Leishmania infantum | 99% | 100% |
D0A2U9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 98% |
E9ASP3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 99% |
Q4Q1V3 | Leishmania major | 96% | 100% |
V5BZP6 | Trypanosoma cruzi | 47% | 100% |