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: 25 |
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: 30 |
NetGPI | no | yes: 0, no: 30 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 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: A4HQK0
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 4 |
GO:0016787 | hydrolase activity | 2 | 4 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 4 |
GO:0016791 | phosphatase activity | 5 | 4 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 4 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 3 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.652 |
CLV_PCSK_FUR_1 | 127 | 131 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 129 | 131 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.631 |
DEG_COP1_1 | 199 | 208 | PF00400 | 0.427 |
DEG_SCF_FBW7_1 | 209 | 216 | PF00400 | 0.463 |
DEG_SPOP_SBC_1 | 99 | 103 | PF00917 | 0.449 |
DOC_CYCLIN_RxL_1 | 136 | 147 | PF00134 | 0.449 |
DOC_MAPK_gen_1 | 197 | 205 | PF00069 | 0.449 |
DOC_MAPK_gen_1 | 57 | 66 | PF00069 | 0.322 |
DOC_MAPK_MEF2A_6 | 57 | 66 | PF00069 | 0.281 |
DOC_PP4_FxxP_1 | 262 | 265 | PF00568 | 0.541 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.798 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.357 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.316 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.593 |
LIG_14-3-3_CanoR_1 | 214 | 221 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 59 | 63 | PF00244 | 0.308 |
LIG_14-3-3_CanoR_1 | 6 | 12 | PF00244 | 0.481 |
LIG_BRCT_BRCA1_1 | 258 | 262 | PF00533 | 0.417 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.350 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.233 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.524 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.626 |
LIG_FHA_1 | 59 | 65 | PF00498 | 0.281 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.440 |
LIG_GBD_Chelix_1 | 62 | 70 | PF00786 | 0.337 |
LIG_LIR_Apic_2 | 259 | 265 | PF02991 | 0.529 |
LIG_LIR_Apic_2 | 46 | 50 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 10 | 14 | PF02991 | 0.559 |
LIG_NRBOX | 183 | 189 | PF00104 | 0.428 |
LIG_PCNA_PIPBox_1 | 84 | 93 | PF02747 | 0.369 |
LIG_Pex14_2 | 258 | 262 | PF04695 | 0.417 |
LIG_SH2_PTP2 | 79 | 82 | PF00017 | 0.356 |
LIG_SH2_SRC | 107 | 110 | PF00017 | 0.356 |
LIG_SH2_STAP1 | 107 | 111 | PF00017 | 0.316 |
LIG_SH2_STAP1 | 164 | 168 | PF00017 | 0.445 |
LIG_SH2_STAT3 | 72 | 75 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 15 | 18 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.427 |
LIG_SH2_STAT5 | 250 | 253 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.273 |
LIG_SH3_1 | 47 | 53 | PF00018 | 0.538 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.601 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.512 |
LIG_SUMO_SIM_par_1 | 149 | 155 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 60 | 65 | PF11976 | 0.309 |
MOD_CDK_SPK_2 | 209 | 214 | PF00069 | 0.547 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.674 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.475 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.433 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.633 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.375 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.559 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.662 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.499 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.552 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.586 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.594 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.637 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.331 |
MOD_N-GLC_1 | 132 | 137 | PF02516 | 0.415 |
MOD_N-GLC_1 | 256 | 261 | PF02516 | 0.723 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.404 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.216 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.595 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.311 |
MOD_NEK2_2 | 180 | 185 | PF00069 | 0.388 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.392 |
MOD_PK_1 | 37 | 43 | PF00069 | 0.642 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.422 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.340 |
MOD_PKB_1 | 5 | 13 | PF00069 | 0.526 |
MOD_Plk_1 | 148 | 154 | PF00069 | 0.342 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.314 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.653 |
MOD_Plk_1 | 66 | 72 | PF00069 | 0.314 |
MOD_Plk_2-3 | 201 | 207 | PF00069 | 0.466 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.319 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.361 |
MOD_Plk_4 | 58 | 64 | PF00069 | 0.321 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.303 |
MOD_Plk_4 | 83 | 89 | PF00069 | 0.356 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.253 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.316 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.525 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.584 |
TRG_DiLeu_BaLyEn_6 | 139 | 144 | PF01217 | 0.456 |
TRG_ER_diArg_1 | 126 | 129 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 270 | 273 | PF00400 | 0.749 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.530 |
TRG_NES_CRM1_1 | 55 | 68 | PF08389 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 142 | 147 | PF00026 | 0.418 |
TRG_Pf-PMV_PEXEL_1 | 192 | 196 | PF00026 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 89 | 93 | PF00026 | 0.419 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7Z9 | Leptomonas seymouri | 74% | 100% |
A0A0N1IKD3 | Leptomonas seymouri | 42% | 100% |
A0A0S4IUQ9 | Bodo saltans | 35% | 81% |
A0A0S4JU61 | Bodo saltans | 52% | 100% |
A0A0S4JWE2 | Bodo saltans | 41% | 100% |
A0A1X0NJT2 | Trypanosomatidae | 42% | 100% |
A0A1X0NLU1 | Trypanosomatidae | 52% | 100% |
A0A1X0P5T3 | Trypanosomatidae | 34% | 92% |
A0A1X0PA23 | Trypanosomatidae | 32% | 83% |
A0A3R7NSE5 | Trypanosoma rangeli | 40% | 100% |
A0A3S7X8P8 | Leishmania donovani | 43% | 100% |
A0A3S7XCG7 | Leishmania donovani | 88% | 100% |
A0A422NVW2 | Trypanosoma rangeli | 52% | 100% |
A4HM58 | Leishmania braziliensis | 43% | 100% |
A4IAS0 | Leishmania infantum | 43% | 100% |
A4ICB8 | Leishmania infantum | 88% | 100% |
C9ZKA3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 69% |
C9ZL07 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 80% |
C9ZZ90 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
D0A2E1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
D0A3Q0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AEA2 | Leishmania major | 37% | 100% |
E9AEJ6 | Leishmania major | 43% | 100% |
E9AUB3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
E9B5Q7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
Q4Q077 | Leishmania major | 88% | 100% |
V5BHN4 | Trypanosoma cruzi | 53% | 100% |
V5BSW0 | Trypanosoma cruzi | 40% | 100% |
V5BX67 | Trypanosoma cruzi | 36% | 79% |