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: 13 |
NetGPI | no | yes: 0, no: 13 |
Related structures:
AlphaFold database: A4IBC9
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0016791 | phosphatase activity | 5 | 1 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 209 | 213 | PF00656 | 0.720 |
CLV_C14_Caspase3-7 | 283 | 287 | PF00656 | 0.503 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.738 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.567 |
CLV_PCSK_FUR_1 | 241 | 245 | PF00082 | 0.665 |
CLV_PCSK_FUR_1 | 298 | 302 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.535 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.488 |
CLV_PCSK_PC1ET2_1 | 36 | 38 | PF00082 | 0.679 |
CLV_PCSK_PC1ET2_1 | 58 | 60 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.672 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.331 |
DEG_APCC_DBOX_1 | 253 | 261 | PF00400 | 0.483 |
DEG_APCC_DBOX_1 | 80 | 88 | PF00400 | 0.315 |
DEG_SCF_FBW7_1 | 187 | 194 | PF00400 | 0.729 |
DOC_CKS1_1 | 188 | 193 | PF01111 | 0.726 |
DOC_CYCLIN_RxL_1 | 248 | 259 | PF00134 | 0.494 |
DOC_CYCLIN_yCln2_LP_2 | 368 | 371 | PF00134 | 0.545 |
DOC_MAPK_gen_1 | 36 | 44 | PF00069 | 0.643 |
DOC_MAPK_gen_1 | 58 | 64 | PF00069 | 0.304 |
DOC_MAPK_gen_1 | 89 | 99 | PF00069 | 0.304 |
DOC_PP2B_LxvP_1 | 368 | 371 | PF13499 | 0.684 |
DOC_PP2B_LxvP_1 | 49 | 52 | PF13499 | 0.469 |
DOC_PP2B_LxvP_1 | 8 | 11 | PF13499 | 0.553 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.760 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 187 | 192 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.728 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.744 |
LIG_14-3-3_CanoR_1 | 241 | 251 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 269 | 277 | PF00244 | 0.517 |
LIG_14-3-3_CanoR_1 | 279 | 283 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 59 | 63 | PF00244 | 0.377 |
LIG_APCC_ABBAyCdc20_2 | 19 | 25 | PF00400 | 0.632 |
LIG_EH1_1 | 118 | 126 | PF00400 | 0.374 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.322 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.359 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.467 |
LIG_FHA_1 | 39 | 45 | PF00498 | 0.690 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.668 |
LIG_FHA_2 | 204 | 210 | PF00498 | 0.773 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.675 |
LIG_FHA_2 | 281 | 287 | PF00498 | 0.550 |
LIG_FHA_2 | 99 | 105 | PF00498 | 0.310 |
LIG_LIR_Gen_1 | 147 | 158 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 172 | 178 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 57 | 66 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 93 | 102 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 172 | 177 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 93 | 98 | PF02991 | 0.315 |
LIG_MYND_1 | 367 | 371 | PF01753 | 0.620 |
LIG_MYND_1 | 6 | 10 | PF01753 | 0.659 |
LIG_NRBOX | 252 | 258 | PF00104 | 0.486 |
LIG_SH2_CRK | 60 | 64 | PF00017 | 0.314 |
LIG_SH2_NCK_1 | 60 | 64 | PF00017 | 0.427 |
LIG_SH2_NCK_1 | 79 | 83 | PF00017 | 0.155 |
LIG_SH2_STAP1 | 107 | 111 | PF00017 | 0.290 |
LIG_SH2_STAP1 | 137 | 141 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 150 | 154 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 60 | 64 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 79 | 83 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.324 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.718 |
LIG_SH3_3 | 324 | 330 | PF00018 | 0.742 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.480 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.748 |
LIG_SUMO_SIM_par_1 | 150 | 155 | PF11976 | 0.294 |
LIG_TRAF2_1 | 180 | 183 | PF00917 | 0.631 |
LIG_TRAF2_2 | 375 | 380 | PF00917 | 0.665 |
LIG_UBA3_1 | 256 | 262 | PF00899 | 0.501 |
LIG_UBA3_1 | 87 | 92 | PF00899 | 0.315 |
MOD_CDC14_SPxK_1 | 238 | 241 | PF00782 | 0.739 |
MOD_CDC14_SPxK_1 | 4 | 7 | PF00782 | 0.673 |
MOD_CDK_SPxK_1 | 1 | 7 | PF00069 | 0.695 |
MOD_CDK_SPxK_1 | 235 | 241 | PF00069 | 0.742 |
MOD_CDK_SPxxK_3 | 235 | 242 | PF00069 | 0.715 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.768 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.415 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.471 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.683 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.728 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.544 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.650 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.776 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.623 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.656 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.310 |
MOD_Cter_Amidation | 45 | 48 | PF01082 | 0.612 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.554 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.672 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.782 |
MOD_GlcNHglycan | 333 | 337 | PF01048 | 0.662 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.663 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.777 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.664 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.748 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.575 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.447 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.543 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.706 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.536 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.522 |
MOD_N-GLC_1 | 148 | 153 | PF02516 | 0.433 |
MOD_N-GLC_1 | 343 | 348 | PF02516 | 0.731 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.433 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.486 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.290 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.763 |
MOD_PKA_1 | 242 | 248 | PF00069 | 0.638 |
MOD_PKA_1 | 58 | 64 | PF00069 | 0.315 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.645 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.378 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.467 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.435 |
MOD_PKB_1 | 241 | 249 | PF00069 | 0.602 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.418 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.415 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.691 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.290 |
MOD_Plk_2-3 | 24 | 30 | PF00069 | 0.588 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.439 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.515 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.593 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.309 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.277 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.659 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.303 |
MOD_ProDKin_1 | 187 | 193 | PF00069 | 0.704 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.728 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.742 |
MOD_SUMO_rev_2 | 20 | 27 | PF00179 | 0.554 |
TRG_DiLeu_BaEn_1 | 39 | 44 | PF01217 | 0.622 |
TRG_DiLeu_BaLyEn_6 | 364 | 369 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 150 | 153 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 60 | 63 | PF00928 | 0.315 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.734 |
TRG_ER_diArg_1 | 298 | 301 | PF00400 | 0.546 |
TRG_ER_diLys_1 | 396 | 401 | PF00400 | 0.618 |
TRG_NES_CRM1_1 | 143 | 155 | PF08389 | 0.408 |
TRG_Pf-PMV_PEXEL_1 | 142 | 147 | PF00026 | 0.396 |
TRG_Pf-PMV_PEXEL_1 | 254 | 258 | PF00026 | 0.491 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1T4 | Leptomonas seymouri | 70% | 96% |
A0A0S4IUQ9 | Bodo saltans | 47% | 100% |
A0A1X0NJT2 | Trypanosomatidae | 33% | 100% |
A0A1X0P5T3 | Trypanosomatidae | 53% | 100% |
A0A3R7P338 | Trypanosoma rangeli | 55% | 100% |
A0A3S7X9F4 | Leishmania donovani | 100% | 100% |
A4HMT1 | Leishmania braziliensis | 80% | 100% |
C9ZZ90 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AF85 | Leishmania major | 95% | 100% |
E9B6E0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 99% |
V5BSW0 | Trypanosoma cruzi | 32% | 100% |
V5BY89 | Trypanosoma cruzi | 54% | 100% |