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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H577
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 |
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 | 7 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 7 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 6 |
GO:0004725 | protein tyrosine phosphatase activity | 4 | 5 |
GO:0008138 | protein tyrosine/serine/threonine phosphatase activity | 4 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0016791 | phosphatase activity | 5 | 7 |
GO:0017018 | myosin phosphatase activity | 5 | 6 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:0008330 | protein tyrosine/threonine phosphatase activity | 4 | 1 |
GO:0017017 | MAP kinase tyrosine/serine/threonine phosphatase activity | 5 | 1 |
GO:0033549 | MAP kinase phosphatase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 262 | 266 | PF00656 | 0.566 |
CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.543 |
CLV_C14_Caspase3-7 | 328 | 332 | PF00656 | 0.530 |
CLV_C14_Caspase3-7 | 425 | 429 | PF00656 | 0.570 |
CLV_C14_Caspase3-7 | 62 | 66 | PF00656 | 0.294 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.621 |
CLV_PCSK_FUR_1 | 205 | 209 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 207 | 209 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 234 | 236 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 229 | 233 | PF00082 | 0.687 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 343 | 347 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 367 | 371 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.562 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.261 |
DEG_SCF_FBW7_1 | 281 | 288 | PF00400 | 0.521 |
DEG_SPOP_SBC_1 | 437 | 441 | PF00917 | 0.523 |
DOC_CKS1_1 | 282 | 287 | PF01111 | 0.518 |
DOC_CYCLIN_RxL_1 | 226 | 233 | PF00134 | 0.695 |
DOC_CYCLIN_yCln2_LP_2 | 296 | 299 | PF00134 | 0.504 |
DOC_MAPK_gen_1 | 148 | 156 | PF00069 | 0.296 |
DOC_MAPK_MEF2A_6 | 150 | 158 | PF00069 | 0.220 |
DOC_MAPK_MEF2A_6 | 180 | 189 | PF00069 | 0.294 |
DOC_PP2B_LxvP_1 | 296 | 299 | PF13499 | 0.504 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.572 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.593 |
DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.575 |
LIG_14-3-3_CanoR_1 | 150 | 155 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 207 | 216 | PF00244 | 0.607 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 276 | 282 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 316 | 324 | PF00244 | 0.530 |
LIG_Actin_RPEL_3 | 143 | 162 | PF02755 | 0.294 |
LIG_BRCT_BRCA1_1 | 362 | 366 | PF00533 | 0.698 |
LIG_BRCT_BRCA1_1 | 399 | 403 | PF00533 | 0.527 |
LIG_CtBP_PxDLS_1 | 298 | 302 | PF00389 | 0.508 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.336 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.469 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.294 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.559 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.423 |
LIG_FHA_1 | 97 | 103 | PF00498 | 0.297 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.585 |
LIG_FHA_2 | 350 | 356 | PF00498 | 0.497 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.662 |
LIG_FHA_2 | 423 | 429 | PF00498 | 0.596 |
LIG_LIR_Gen_1 | 206 | 216 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 56 | 63 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 206 | 212 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 363 | 369 | PF02991 | 0.707 |
LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 86 | 91 | PF02991 | 0.349 |
LIG_PCNA_PIPBox_1 | 225 | 234 | PF02747 | 0.413 |
LIG_PCNA_yPIPBox_3 | 225 | 235 | PF02747 | 0.416 |
LIG_PDZ_Class_2 | 445 | 450 | PF00595 | 0.566 |
LIG_REV1ctd_RIR_1 | 348 | 358 | PF16727 | 0.539 |
LIG_SH2_GRB2like | 163 | 166 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.207 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.730 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.183 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.764 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.679 |
LIG_SUMO_SIM_anti_2 | 153 | 158 | PF11976 | 0.220 |
LIG_TRAF2_1 | 201 | 204 | PF00917 | 0.482 |
LIG_TRAF2_1 | 443 | 446 | PF00917 | 0.523 |
LIG_TRAF2_1 | 84 | 87 | PF00917 | 0.294 |
LIG_WRC_WIRS_1 | 97 | 102 | PF05994 | 0.294 |
LIG_WW_3 | 32 | 36 | PF00397 | 0.534 |
MOD_CDC14_SPxK_1 | 32 | 35 | PF00782 | 0.660 |
MOD_CDC14_SPxK_1 | 334 | 337 | PF00782 | 0.531 |
MOD_CDK_SPxK_1 | 29 | 35 | PF00069 | 0.664 |
MOD_CDK_SPxK_1 | 301 | 307 | PF00069 | 0.521 |
MOD_CDK_SPxK_1 | 331 | 337 | PF00069 | 0.536 |
MOD_CDK_SPxxK_3 | 198 | 205 | PF00069 | 0.391 |
MOD_CDK_SPxxK_3 | 320 | 327 | PF00069 | 0.530 |
MOD_CDK_SPxxK_3 | 331 | 338 | PF00069 | 0.510 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.297 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.443 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.624 |
MOD_CK1_1 | 422 | 428 | PF00069 | 0.555 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.566 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.299 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.512 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.549 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.294 |
MOD_GlcNHglycan | 103 | 107 | PF01048 | 0.294 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.545 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.641 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.628 |
MOD_GlcNHglycan | 35 | 38 | PF01048 | 0.575 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.619 |
MOD_GlcNHglycan | 399 | 402 | PF01048 | 0.501 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.483 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.311 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.294 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.646 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.482 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.681 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.618 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.658 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.573 |
MOD_GSK3_1 | 395 | 402 | PF00069 | 0.544 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.541 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.444 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.337 |
MOD_N-GLC_1 | 9 | 14 | PF02516 | 0.516 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.344 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.294 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.419 |
MOD_NEK2_1 | 277 | 282 | PF00069 | 0.702 |
MOD_NEK2_2 | 59 | 64 | PF00069 | 0.345 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.561 |
MOD_OFUCOSY | 347 | 353 | PF10250 | 0.489 |
MOD_PIKK_1 | 223 | 229 | PF00454 | 0.511 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.536 |
MOD_PIKK_1 | 49 | 55 | PF00454 | 0.363 |
MOD_PIKK_1 | 81 | 87 | PF00454 | 0.294 |
MOD_PIKK_1 | 9 | 15 | PF00454 | 0.642 |
MOD_PK_1 | 150 | 156 | PF00069 | 0.220 |
MOD_PKA_1 | 207 | 213 | PF00069 | 0.470 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.470 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.741 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.565 |
MOD_PKB_1 | 150 | 158 | PF00069 | 0.294 |
MOD_PKB_1 | 205 | 213 | PF00069 | 0.526 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.549 |
MOD_Plk_1 | 444 | 450 | PF00069 | 0.541 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.517 |
MOD_Plk_2-3 | 87 | 93 | PF00069 | 0.294 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.311 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.556 |
MOD_Plk_4 | 285 | 291 | PF00069 | 0.618 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.581 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.581 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.387 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.558 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.520 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.591 |
MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.483 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.538 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.548 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.578 |
MOD_SUMO_rev_2 | 86 | 95 | PF00179 | 0.345 |
TRG_DiLeu_BaEn_2 | 210 | 216 | PF01217 | 0.529 |
TRG_DiLeu_BaEn_4 | 191 | 197 | PF01217 | 0.294 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.329 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.345 |
TRG_ER_diArg_1 | 179 | 181 | PF00400 | 0.349 |
TRG_ER_diArg_1 | 205 | 208 | PF00400 | 0.552 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.653 |
TRG_Pf-PMV_PEXEL_1 | 194 | 198 | PF00026 | 0.351 |
TRG_Pf-PMV_PEXEL_1 | 217 | 222 | PF00026 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.579 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P9F6 | Leptomonas seymouri | 53% | 85% |
A0A3S5H628 | Leishmania donovani | 76% | 100% |
A4HTG0 | Leishmania infantum | 75% | 100% |
E9AM88 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4QIF9 | Leishmania major | 75% | 100% |