Phosphatase, Serine/threonine phosphatases Stage II sporulation E (SpoIIE), putative
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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0016020 | membrane | 2 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4I1Q4
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 13 |
GO:0004722 | protein serine/threonine phosphatase activity | 4 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 13 |
GO:0016791 | phosphatase activity | 5 | 13 |
GO:0017018 | myosin phosphatase activity | 5 | 13 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043169 | cation binding | 3 | 13 |
GO:0046872 | metal ion binding | 4 | 13 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 353 | 359 | PF00089 | 0.251 |
CLV_NRD_NRD_1 | 175 | 177 | PF00675 | 0.236 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.213 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.353 |
CLV_PCSK_FUR_1 | 73 | 77 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.404 |
CLV_PCSK_PC1ET2_1 | 74 | 76 | PF00082 | 0.416 |
CLV_PCSK_PC1ET2_1 | 83 | 85 | PF00082 | 0.381 |
CLV_PCSK_SKI1_1 | 156 | 160 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.294 |
DEG_SPOP_SBC_1 | 165 | 169 | PF00917 | 0.422 |
DOC_CKS1_1 | 31 | 36 | PF01111 | 0.572 |
DOC_CKS1_1 | 8 | 13 | PF01111 | 0.533 |
DOC_MAPK_gen_1 | 156 | 165 | PF00069 | 0.493 |
DOC_MAPK_gen_1 | 343 | 352 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 82 | 90 | PF00069 | 0.395 |
DOC_MAPK_MEF2A_6 | 346 | 354 | PF00069 | 0.422 |
DOC_PP4_FxxP_1 | 214 | 217 | PF00568 | 0.402 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.402 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.570 |
DOC_WW_Pin1_4 | 325 | 330 | PF00397 | 0.400 |
DOC_WW_Pin1_4 | 58 | 63 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 7 | 12 | PF00397 | 0.534 |
LIG_14-3-3_CanoR_1 | 356 | 363 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 4 | 8 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 75 | 80 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 82 | 88 | PF00244 | 0.383 |
LIG_BIR_III_4 | 341 | 345 | PF00653 | 0.402 |
LIG_BRCT_BRCA1_1 | 51 | 55 | PF00533 | 0.395 |
LIG_BRCT_BRCA1_2 | 51 | 57 | PF00533 | 0.400 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.468 |
LIG_FHA_1 | 167 | 173 | PF00498 | 0.333 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.434 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.415 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.487 |
LIG_FHA_2 | 31 | 37 | PF00498 | 0.557 |
LIG_FHA_2 | 357 | 363 | PF00498 | 0.328 |
LIG_LIR_Apic_2 | 30 | 34 | PF02991 | 0.477 |
LIG_LIR_Apic_2 | 302 | 306 | PF02991 | 0.451 |
LIG_LIR_Gen_1 | 151 | 162 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 328 | 337 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 86 | 94 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 202 | 207 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.388 |
LIG_Pex14_2 | 214 | 218 | PF04695 | 0.402 |
LIG_Pex14_2 | 260 | 264 | PF04695 | 0.422 |
LIG_RPA_C_Fungi | 258 | 270 | PF08784 | 0.322 |
LIG_SH2_CRK | 103 | 107 | PF00017 | 0.254 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.349 |
LIG_SH2_PTP2 | 303 | 306 | PF00017 | 0.283 |
LIG_SH2_SRC | 303 | 306 | PF00017 | 0.283 |
LIG_SH2_STAP1 | 154 | 158 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 303 | 306 | PF00017 | 0.246 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.626 |
LIG_SH3_4 | 59 | 66 | PF00018 | 0.553 |
LIG_SPRY_1 | 362 | 367 | PF00622 | 0.505 |
LIG_SUMO_SIM_anti_2 | 192 | 199 | PF11976 | 0.283 |
LIG_SUMO_SIM_anti_2 | 250 | 257 | PF11976 | 0.322 |
LIG_SUMO_SIM_anti_2 | 348 | 355 | PF11976 | 0.284 |
LIG_SUMO_SIM_par_1 | 348 | 355 | PF11976 | 0.284 |
LIG_TRAF2_1 | 245 | 248 | PF00917 | 0.325 |
LIG_TRAF2_1 | 359 | 362 | PF00917 | 0.367 |
LIG_TRAF2_2 | 245 | 250 | PF00917 | 0.370 |
MOD_CDK_SPxK_1 | 58 | 64 | PF00069 | 0.472 |
MOD_CDK_SPxxK_3 | 278 | 285 | PF00069 | 0.403 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.613 |
MOD_CK1_1 | 355 | 361 | PF00069 | 0.350 |
MOD_CK2_1 | 355 | 361 | PF00069 | 0.322 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.392 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.606 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.583 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.254 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.292 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.517 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.280 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.272 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.486 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.336 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.322 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.269 |
MOD_NEK2_2 | 171 | 176 | PF00069 | 0.381 |
MOD_NEK2_2 | 93 | 98 | PF00069 | 0.284 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.568 |
MOD_PK_1 | 75 | 81 | PF00069 | 0.476 |
MOD_PKA_1 | 75 | 81 | PF00069 | 0.386 |
MOD_PKA_1 | 83 | 89 | PF00069 | 0.393 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.299 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.656 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.321 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.382 |
MOD_PKA_2 | 83 | 89 | PF00069 | 0.393 |
MOD_PKB_1 | 73 | 81 | PF00069 | 0.392 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.254 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.273 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.317 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.242 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.396 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.276 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.406 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.577 |
MOD_ProDKin_1 | 325 | 331 | PF00069 | 0.251 |
MOD_ProDKin_1 | 58 | 64 | PF00069 | 0.403 |
MOD_ProDKin_1 | 7 | 13 | PF00069 | 0.532 |
MOD_SUMO_for_1 | 299 | 302 | PF00179 | 0.327 |
MOD_SUMO_rev_2 | 294 | 301 | PF00179 | 0.269 |
MOD_SUMO_rev_2 | 36 | 45 | PF00179 | 0.470 |
TRG_DiLeu_BaEn_2 | 93 | 99 | PF01217 | 0.284 |
TRG_ENDOCYTIC_2 | 103 | 106 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.291 |
TRG_ER_diArg_1 | 198 | 201 | PF00400 | 0.267 |
TRG_ER_diArg_1 | 73 | 76 | PF00400 | 0.409 |
TRG_ER_diArg_1 | 81 | 84 | PF00400 | 0.357 |
TRG_NLS_MonoExtN_4 | 73 | 78 | PF00514 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 312 | 316 | PF00026 | 0.403 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2Z6 | Leptomonas seymouri | 82% | 100% |
A0A0N1IH92 | Leptomonas seymouri | 27% | 100% |
A0A0S4IN49 | Bodo saltans | 36% | 100% |
A0A0S4JF75 | Bodo saltans | 24% | 70% |
A0A0S4JK95 | Bodo saltans | 63% | 100% |
A0A0S4JS91 | Bodo saltans | 63% | 100% |
A0A1X0NY52 | Trypanosomatidae | 62% | 97% |
A0A1X0P4F0 | Trypanosomatidae | 26% | 100% |
A0A1X0P973 | Trypanosomatidae | 28% | 100% |
A0A3Q8IBW1 | Leishmania donovani | 100% | 100% |
A0A3R7N5R3 | Trypanosoma rangeli | 28% | 100% |
A0A3R7RFR7 | Trypanosoma rangeli | 29% | 100% |
A0A422P4L0 | Trypanosoma rangeli | 68% | 100% |
A4HEA8 | Leishmania braziliensis | 94% | 100% |
B3MTI8 | Drosophila ananassae | 34% | 100% |
B3P5D3 | Drosophila erecta | 36% | 100% |
B4G653 | Drosophila persimilis | 34% | 100% |
B4HZE7 | Drosophila sechellia | 36% | 100% |
B4JYN1 | Drosophila grimshawi | 35% | 100% |
B4K616 | Drosophila mojavensis | 38% | 100% |
B4M5T5 | Drosophila virilis | 37% | 100% |
B4NBL6 | Drosophila willistoni | 38% | 100% |
B4PPK3 | Drosophila yakuba | 36% | 100% |
B4R089 | Drosophila simulans | 36% | 100% |
C9ZKA8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 66% | 100% |
C9ZN10 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
D0A5X5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AXT8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O64730 | Arabidopsis thaliana | 32% | 100% |
P38797 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 32% | 100% |
Q09189 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
Q29AP0 | Drosophila pseudoobscura pseudoobscura | 35% | 100% |
Q339D2 | Oryza sativa subsp. japonica | 31% | 79% |
Q4Q9N3 | Leishmania major | 96% | 100% |
Q5U3N5 | Danio rerio | 37% | 100% |
Q6GR25 | Xenopus laevis | 37% | 100% |
Q6H7J3 | Oryza sativa subsp. japonica | 32% | 100% |
Q6H7J4 | Oryza sativa subsp. japonica | 28% | 100% |
Q6NVE9 | Mus musculus | 38% | 100% |
Q8NI37 | Homo sapiens | 38% | 100% |
Q942P9 | Oryza sativa subsp. japonica | 31% | 100% |
Q9LVQ8 | Arabidopsis thaliana | 34% | 89% |
Q9SUK9 | Arabidopsis thaliana | 33% | 79% |
Q9VAH4 | Drosophila melanogaster | 36% | 100% |
V5AT69 | Trypanosoma cruzi | 27% | 100% |
V5AUW7 | Trypanosoma cruzi | 31% | 100% |
V5BMI3 | Trypanosoma cruzi | 65% | 85% |