A metalloenzyme with the catalytic domain facing outwards. Related to plant Shewanella-like protein phosphatases. Kinetoplastids have multiple copies of these genes but probably from a very ancient gene duplication.. The cluster might merge two separate, very distantly related groups.
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 11, no: 14 |
NetGPI | no | yes: 0, no: 25 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
Related structures:
AlphaFold database: A4HIR7
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 26 |
GO:0016787 | hydrolase activity | 2 | 26 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.260 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.273 |
CLV_PCSK_FUR_1 | 202 | 206 | PF00082 | 0.252 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.243 |
CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.238 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.170 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.447 |
DEG_APCC_DBOX_1 | 317 | 325 | PF00400 | 0.203 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.382 |
DOC_CYCLIN_RxL_1 | 240 | 249 | PF00134 | 0.193 |
DOC_MAPK_gen_1 | 315 | 324 | PF00069 | 0.210 |
DOC_MAPK_gen_1 | 47 | 55 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 57 | 64 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 318 | 326 | PF00069 | 0.378 |
DOC_MAPK_MEF2A_6 | 57 | 64 | PF00069 | 0.445 |
DOC_MAPK_RevD_3 | 189 | 205 | PF00069 | 0.374 |
DOC_MAPK_RevD_3 | 68 | 83 | PF00069 | 0.293 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.639 |
DOC_USP7_UBL2_3 | 287 | 291 | PF12436 | 0.259 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.257 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.366 |
LIG_14-3-3_CanoR_1 | 19 | 28 | PF00244 | 0.352 |
LIG_14-3-3_CanoR_1 | 2 | 12 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 51 | 56 | PF00244 | 0.464 |
LIG_BRCT_BRCA1_1 | 16 | 20 | PF00533 | 0.385 |
LIG_Clathr_ClatBox_1 | 321 | 325 | PF01394 | 0.276 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.430 |
LIG_FHA_1 | 403 | 409 | PF00498 | 0.695 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.478 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.291 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.310 |
LIG_Integrin_RGD_1 | 167 | 169 | PF01839 | 0.298 |
LIG_LIR_Nem_3 | 169 | 173 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.273 |
LIG_MYND_1 | 406 | 410 | PF01753 | 0.524 |
LIG_SH2_NCK_1 | 40 | 44 | PF00017 | 0.350 |
LIG_SH2_STAP1 | 40 | 44 | PF00017 | 0.350 |
LIG_SH2_STAP1 | 94 | 98 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.673 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.233 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.338 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.480 |
LIG_SUMO_SIM_anti_2 | 132 | 138 | PF11976 | 0.444 |
LIG_SUMO_SIM_anti_2 | 97 | 102 | PF11976 | 0.483 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.243 |
LIG_SUMO_SIM_par_1 | 320 | 325 | PF11976 | 0.262 |
LIG_SUMO_SIM_par_1 | 59 | 65 | PF11976 | 0.333 |
LIG_SUMO_SIM_par_1 | 69 | 74 | PF11976 | 0.359 |
LIG_SUMO_SIM_par_1 | 75 | 80 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 83 | 89 | PF11976 | 0.479 |
LIG_TYR_ITIM | 417 | 422 | PF00017 | 0.399 |
LIG_UBA3_1 | 227 | 233 | PF00899 | 0.318 |
MOD_CDC14_SPxK_1 | 11 | 14 | PF00782 | 0.445 |
MOD_CDK_SPxK_1 | 8 | 14 | PF00069 | 0.449 |
MOD_CDK_SPxxK_3 | 248 | 255 | PF00069 | 0.409 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.288 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.272 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.244 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.682 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.659 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.298 |
MOD_Cter_Amidation | 48 | 51 | PF01082 | 0.421 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.396 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.551 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.262 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.445 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.303 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.598 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.350 |
MOD_N-GLC_1 | 192 | 197 | PF02516 | 0.291 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.342 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.315 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.329 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.352 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.349 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.296 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.334 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.446 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.342 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.330 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.398 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.438 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.220 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.309 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.516 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.722 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.322 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.296 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.473 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.470 |
MOD_ProDKin_1 | 8 | 14 | PF00069 | 0.449 |
MOD_SUMO_rev_2 | 286 | 294 | PF00179 | 0.331 |
TRG_DiLeu_BaEn_1 | 116 | 121 | PF01217 | 0.409 |
TRG_DiLeu_BaEn_1 | 80 | 85 | PF01217 | 0.301 |
TRG_DiLeu_BaLyEn_6 | 102 | 107 | PF01217 | 0.247 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.354 |
TRG_DiLeu_BaLyEn_6 | 27 | 32 | PF01217 | 0.527 |
TRG_DiLeu_BaLyEn_6 | 317 | 322 | PF01217 | 0.331 |
TRG_DiLeu_BaLyEn_6 | 407 | 412 | PF01217 | 0.464 |
TRG_DiLeu_BaLyEn_6 | 58 | 63 | PF01217 | 0.485 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.379 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 419 | 422 | PF00928 | 0.513 |
TRG_ER_diArg_1 | 201 | 204 | PF00400 | 0.266 |
TRG_ER_diArg_1 | 318 | 321 | PF00400 | 0.239 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.277 |
TRG_NES_CRM1_1 | 132 | 146 | PF08389 | 0.209 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3V2 | Leptomonas seymouri | 74% | 100% |
A0A0N1P9R1 | Leptomonas seymouri | 27% | 100% |
A0A0S4JBT9 | Bodo saltans | 33% | 100% |
A0A0S4KJG1 | Bodo saltans | 58% | 100% |
A0A1X0NU01 | Trypanosomatidae | 25% | 100% |
A0A3Q8IBB4 | Leishmania donovani | 28% | 100% |
A0A3Q8IIK0 | Leishmania donovani | 29% | 100% |
A0A3R7NTC0 | Trypanosoma rangeli | 63% | 100% |
A0A3S7X3U9 | Leishmania donovani | 81% | 100% |
A4HCJ2 | Leishmania braziliensis | 28% | 100% |
A4HH45 | Leishmania braziliensis | 29% | 100% |
A4I008 | Leishmania infantum | 28% | 100% |
A4I498 | Leishmania infantum | 29% | 100% |
A4I612 | Leishmania infantum | 82% | 100% |
C9ZQ86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
C9ZRD7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 95% |
E9ADP5 | Leishmania major | 29% | 100% |
E9AM35 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AVY1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
E9B1A3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q6W1 | Leishmania major | 81% | 100% |
Q4QBJ8 | Leishmania major | 28% | 100% |
V5ARZ9 | Trypanosoma cruzi | 25% | 100% |
V5BX32 | Trypanosoma cruzi | 57% | 100% |