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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7XBA9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.439 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.747 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.597 |
CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.445 |
CLV_PCSK_KEX2_1 | 219 | 221 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 67 | 69 | PF00082 | 0.700 |
CLV_PCSK_PC1ET2_1 | 130 | 132 | PF00082 | 0.440 |
CLV_PCSK_PC1ET2_1 | 67 | 69 | PF00082 | 0.751 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.425 |
DEG_APCC_DBOX_1 | 33 | 41 | PF00400 | 0.609 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.598 |
DEG_SPOP_SBC_1 | 90 | 94 | PF00917 | 0.697 |
DOC_MAPK_gen_1 | 187 | 193 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 19 | 27 | PF00069 | 0.710 |
DOC_PP1_RVXF_1 | 115 | 121 | PF00149 | 0.560 |
DOC_PP1_RVXF_1 | 65 | 72 | PF00149 | 0.659 |
DOC_PP2B_LxvP_1 | 272 | 275 | PF13499 | 0.593 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.789 |
DOC_USP7_UBL2_3 | 188 | 192 | PF12436 | 0.455 |
DOC_USP7_UBL2_3 | 57 | 61 | PF12436 | 0.680 |
DOC_WW_Pin1_4 | 111 | 116 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.634 |
LIG_14-3-3_CanoR_1 | 117 | 121 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 131 | 135 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 219 | 227 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 45 | 53 | PF00244 | 0.620 |
LIG_APCC_ABBAyCdc20_2 | 152 | 158 | PF00400 | 0.429 |
LIG_BRCT_BRCA1_1 | 7 | 11 | PF00533 | 0.600 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.563 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.710 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.504 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.588 |
LIG_FHA_2 | 92 | 98 | PF00498 | 0.726 |
LIG_LIR_Gen_1 | 122 | 129 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 153 | 164 | PF02991 | 0.527 |
LIG_LIR_Gen_1 | 168 | 176 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 248 | 257 | PF02991 | 0.705 |
LIG_LIR_Gen_1 | 3 | 11 | PF02991 | 0.547 |
LIG_LIR_Nem_3 | 119 | 123 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 133 | 137 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 146 | 150 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 153 | 159 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 168 | 172 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.541 |
LIG_LIR_Nem_3 | 300 | 306 | PF02991 | 0.576 |
LIG_Pex14_1 | 147 | 151 | PF04695 | 0.477 |
LIG_Pex14_2 | 71 | 75 | PF04695 | 0.648 |
LIG_Pex14_2 | 9 | 13 | PF04695 | 0.459 |
LIG_SH2_CRK | 137 | 141 | PF00017 | 0.513 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.638 |
LIG_SH2_GRB2like | 164 | 167 | PF00017 | 0.499 |
LIG_SH2_SRC | 156 | 159 | PF00017 | 0.479 |
LIG_SH2_STAT3 | 121 | 124 | PF00017 | 0.694 |
LIG_SH2_STAT3 | 164 | 167 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.753 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.718 |
LIG_TRAF2_1 | 110 | 113 | PF00917 | 0.599 |
LIG_TRAF2_1 | 210 | 213 | PF00917 | 0.519 |
LIG_TYR_ITIM | 249 | 254 | PF00017 | 0.625 |
LIG_UBA3_1 | 293 | 301 | PF00899 | 0.584 |
LIG_ULM_U2AF65_1 | 180 | 185 | PF00076 | 0.418 |
MOD_CDC14_SPxK_1 | 127 | 130 | PF00782 | 0.477 |
MOD_CDK_SPxK_1 | 111 | 117 | PF00069 | 0.571 |
MOD_CDK_SPxK_1 | 124 | 130 | PF00069 | 0.484 |
MOD_CDK_SPxxK_3 | 124 | 131 | PF00069 | 0.503 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.636 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.652 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.562 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.498 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.605 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.774 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.718 |
MOD_GlcNHglycan | 158 | 162 | PF01048 | 0.552 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.597 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.722 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.778 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.571 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.614 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.515 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.576 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.715 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.472 |
MOD_NEK2_1 | 239 | 244 | PF00069 | 0.719 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.697 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.715 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.547 |
MOD_OFUCOSY | 44 | 49 | PF10250 | 0.658 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.629 |
MOD_PKA_1 | 130 | 136 | PF00069 | 0.485 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.544 |
MOD_PKA_2 | 130 | 136 | PF00069 | 0.465 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.507 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.751 |
MOD_PKB_1 | 308 | 316 | PF00069 | 0.632 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.470 |
MOD_Plk_1 | 193 | 199 | PF00069 | 0.512 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.580 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.537 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.512 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.745 |
MOD_ProDKin_1 | 111 | 117 | PF00069 | 0.571 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.484 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.633 |
MOD_SUMO_rev_2 | 295 | 302 | PF00179 | 0.662 |
MOD_SUMO_rev_2 | 59 | 69 | PF00179 | 0.733 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.662 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.636 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.442 |
TRG_ER_diArg_1 | 307 | 310 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 51 | 53 | PF00400 | 0.717 |
TRG_Pf-PMV_PEXEL_1 | 138 | 142 | PF00026 | 0.445 |
TRG_Pf-PMV_PEXEL_1 | 39 | 43 | PF00026 | 0.631 |
TRG_Pf-PMV_PEXEL_1 | 45 | 50 | PF00026 | 0.558 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4T7 | Leptomonas seymouri | 76% | 100% |
A0A1X0P4T0 | Trypanosomatidae | 78% | 98% |
A4HPN4 | Leishmania braziliensis | 85% | 100% |
A4ID30 | Leishmania infantum | 99% | 100% |
D0A8H9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 68% | 100% |
E9ATE8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q149 | Leishmania major | 93% | 100% |
V5BIQ3 | Trypanosoma cruzi | 78% | 96% |