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:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HP87
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 | 7 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 7 |
GO:0004725 | protein tyrosine 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:0042578 | phosphoric ester hydrolase activity | 4 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 2 | 6 | PF00656 | 0.466 |
CLV_C14_Caspase3-7 | 356 | 360 | PF00656 | 0.202 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.202 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.344 |
CLV_NRD_NRD_1 | 449 | 451 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 484 | 486 | PF00675 | 0.435 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 223 | 225 | PF00082 | 0.202 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.344 |
CLV_PCSK_KEX2_1 | 449 | 451 | PF00082 | 0.344 |
CLV_PCSK_PC1ET2_1 | 195 | 197 | PF00082 | 0.338 |
CLV_PCSK_PC1ET2_1 | 223 | 225 | PF00082 | 0.202 |
CLV_PCSK_PC7_1 | 220 | 226 | PF00082 | 0.202 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 514 | 518 | PF00082 | 0.439 |
CLV_Separin_Metazoa | 320 | 324 | PF03568 | 0.344 |
DEG_SPOP_SBC_1 | 392 | 396 | PF00917 | 0.202 |
DOC_CYCLIN_RxL_1 | 191 | 200 | PF00134 | 0.334 |
DOC_CYCLIN_RxL_1 | 505 | 512 | PF00134 | 0.312 |
DOC_CYCLIN_yCln2_LP_2 | 410 | 416 | PF00134 | 0.344 |
DOC_MAPK_gen_1 | 406 | 416 | PF00069 | 0.201 |
DOC_MAPK_MEF2A_6 | 409 | 416 | PF00069 | 0.284 |
DOC_MAPK_MEF2A_6 | 465 | 474 | PF00069 | 0.280 |
DOC_MAPK_RevD_3 | 470 | 486 | PF00069 | 0.391 |
DOC_PP2B_LxvP_1 | 410 | 413 | PF13499 | 0.344 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.284 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.336 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.202 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.653 |
DOC_USP7_UBL2_3 | 191 | 195 | PF12436 | 0.320 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.501 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.344 |
DOC_WW_Pin1_4 | 69 | 74 | PF00397 | 0.546 |
LIG_14-3-3_CanoR_1 | 196 | 202 | PF00244 | 0.330 |
LIG_14-3-3_CanoR_1 | 485 | 493 | PF00244 | 0.416 |
LIG_AP_GAE_1 | 105 | 111 | PF02883 | 0.434 |
LIG_APCC_ABBA_1 | 303 | 308 | PF00400 | 0.280 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.619 |
LIG_BRCT_BRCA1_1 | 202 | 206 | PF00533 | 0.361 |
LIG_BRCT_BRCA1_2 | 202 | 208 | PF00533 | 0.381 |
LIG_CtBP_PxDLS_1 | 169 | 173 | PF00389 | 0.621 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.344 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.242 |
LIG_FHA_1 | 316 | 322 | PF00498 | 0.290 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.382 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.252 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.297 |
LIG_FHA_2 | 399 | 405 | PF00498 | 0.290 |
LIG_LIR_Gen_1 | 255 | 262 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 358 | 368 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 467 | 477 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 98 | 109 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 255 | 260 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 467 | 472 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 98 | 104 | PF02991 | 0.326 |
LIG_NRP_CendR_1 | 517 | 518 | PF00754 | 0.520 |
LIG_PCNA_PIPBox_1 | 251 | 260 | PF02747 | 0.344 |
LIG_PTAP_UEV_1 | 374 | 379 | PF05743 | 0.202 |
LIG_PTB_Apo_2 | 84 | 91 | PF02174 | 0.458 |
LIG_SH2_CRK | 344 | 348 | PF00017 | 0.344 |
LIG_SH2_CRK | 432 | 436 | PF00017 | 0.280 |
LIG_SH2_CRK | 469 | 473 | PF00017 | 0.280 |
LIG_SH2_GRB2like | 135 | 138 | PF00017 | 0.405 |
LIG_SH2_GRB2like | 229 | 232 | PF00017 | 0.280 |
LIG_SH2_PTP2 | 135 | 138 | PF00017 | 0.405 |
LIG_SH2_PTP2 | 327 | 330 | PF00017 | 0.344 |
LIG_SH2_SRC | 135 | 138 | PF00017 | 0.405 |
LIG_SH2_SRC | 229 | 232 | PF00017 | 0.344 |
LIG_SH2_SRC | 344 | 347 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 262 | 266 | PF00017 | 0.344 |
LIG_SH2_STAP1 | 313 | 317 | PF00017 | 0.280 |
LIG_SH2_STAT3 | 306 | 309 | PF00017 | 0.202 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.280 |
LIG_SH2_STAT5 | 346 | 349 | PF00017 | 0.167 |
LIG_SH2_STAT5 | 371 | 374 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 432 | 435 | PF00017 | 0.280 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.524 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.340 |
LIG_SH3_3 | 344 | 350 | PF00018 | 0.344 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.295 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.236 |
LIG_SUMO_SIM_anti_2 | 255 | 263 | PF11976 | 0.344 |
LIG_SUMO_SIM_anti_2 | 265 | 270 | PF11976 | 0.251 |
LIG_SUMO_SIM_par_1 | 10 | 17 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 267 | 274 | PF11976 | 0.284 |
LIG_TRAF2_1 | 140 | 143 | PF00917 | 0.354 |
LIG_TRAF2_1 | 249 | 252 | PF00917 | 0.344 |
LIG_TRAF2_1 | 360 | 363 | PF00917 | 0.280 |
LIG_TRAF2_1 | 96 | 99 | PF00917 | 0.533 |
LIG_TYR_ITIM | 342 | 347 | PF00017 | 0.344 |
LIG_WRC_WIRS_1 | 297 | 302 | PF05994 | 0.279 |
MOD_CDK_SPK_2 | 157 | 162 | PF00069 | 0.544 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.563 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.594 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.370 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.563 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.519 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.344 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.280 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.244 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.660 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.601 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.280 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.280 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.568 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.609 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.413 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.582 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.715 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.370 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.285 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.322 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.460 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.262 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.524 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.423 |
MOD_GlcNHglycan | 52 | 56 | PF01048 | 0.594 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.598 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.615 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.465 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.626 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.289 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.666 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.356 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.290 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.178 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.403 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.532 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.554 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.358 |
MOD_N-GLC_1 | 26 | 31 | PF02516 | 0.563 |
MOD_N-GLC_1 | 3 | 8 | PF02516 | 0.529 |
MOD_N-GLC_1 | 398 | 403 | PF02516 | 0.268 |
MOD_N-GLC_1 | 444 | 449 | PF02516 | 0.344 |
MOD_N-GLC_1 | 57 | 62 | PF02516 | 0.509 |
MOD_N-GLC_1 | 77 | 82 | PF02516 | 0.519 |
MOD_N-GLC_2 | 302 | 304 | PF02516 | 0.202 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.397 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.692 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.504 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.401 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.276 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.344 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.503 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.623 |
MOD_NEK2_2 | 175 | 180 | PF00069 | 0.427 |
MOD_NEK2_2 | 444 | 449 | PF00069 | 0.202 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.280 |
MOD_PKA_1 | 485 | 491 | PF00069 | 0.427 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.204 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.306 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.202 |
MOD_Plk_1 | 141 | 147 | PF00069 | 0.386 |
MOD_Plk_1 | 235 | 241 | PF00069 | 0.344 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.579 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.458 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.618 |
MOD_Plk_1 | 444 | 450 | PF00069 | 0.344 |
MOD_Plk_1 | 57 | 63 | PF00069 | 0.508 |
MOD_Plk_2-3 | 311 | 317 | PF00069 | 0.254 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.354 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.326 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.343 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.280 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.502 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.622 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.737 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.344 |
MOD_ProDKin_1 | 69 | 75 | PF00069 | 0.546 |
MOD_SUMO_rev_2 | 106 | 116 | PF00179 | 0.305 |
TRG_DiLeu_BaEn_1 | 265 | 270 | PF01217 | 0.202 |
TRG_DiLeu_BaEn_1 | 99 | 104 | PF01217 | 0.360 |
TRG_DiLeu_BaEn_2 | 275 | 281 | PF01217 | 0.344 |
TRG_DiLeu_BaEn_2 | 466 | 472 | PF01217 | 0.280 |
TRG_DiLeu_BaEn_3 | 362 | 368 | PF01217 | 0.280 |
TRG_DiLeu_BaLyEn_6 | 193 | 198 | PF01217 | 0.330 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 344 | 347 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 432 | 435 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 469 | 472 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 473 | 476 | PF00928 | 0.280 |
TRG_ER_diArg_1 | 224 | 226 | PF00400 | 0.202 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 448 | 450 | PF00400 | 0.344 |
TRG_NLS_MonoExtN_4 | 220 | 227 | PF00514 | 0.202 |
TRG_Pf-PMV_PEXEL_1 | 508 | 512 | PF00026 | 0.310 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILN6 | Leptomonas seymouri | 50% | 100% |
A0A3S7XAX7 | Leishmania donovani | 73% | 99% |
A4IDJ2 | Leishmania infantum | 73% | 99% |
E9ASZ5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 99% |
P34138 | Dictyostelium discoideum | 24% | 100% |
Q4Q1K3 | Leishmania major | 75% | 100% |