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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HDQ6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.487 |
CLV_PCSK_FUR_1 | 281 | 285 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 134 | 136 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 134 | 136 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 195 | 199 | PF00082 | 0.434 |
DEG_APCC_DBOX_1 | 291 | 299 | PF00400 | 0.546 |
DEG_SPOP_SBC_1 | 123 | 127 | PF00917 | 0.831 |
DEG_SPOP_SBC_1 | 352 | 356 | PF00917 | 0.342 |
DEG_SPOP_SBC_1 | 54 | 58 | PF00917 | 0.822 |
DOC_ANK_TNKS_1 | 41 | 48 | PF00023 | 0.652 |
DOC_MAPK_HePTP_8 | 216 | 228 | PF00069 | 0.633 |
DOC_MAPK_HePTP_8 | 258 | 270 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 219 | 228 | PF00069 | 0.630 |
DOC_MAPK_MEF2A_6 | 261 | 270 | PF00069 | 0.654 |
DOC_PP2B_PxIxI_1 | 78 | 84 | PF00149 | 0.659 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 253 | 257 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.777 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.635 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.261 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.736 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.779 |
LIG_14-3-3_CanoR_1 | 292 | 298 | PF00244 | 0.411 |
LIG_14-3-3_CanoR_1 | 42 | 46 | PF00244 | 0.748 |
LIG_14-3-3_CanoR_1 | 68 | 74 | PF00244 | 0.748 |
LIG_Actin_RPEL_3 | 239 | 258 | PF02755 | 0.621 |
LIG_Actin_WH2_2 | 255 | 271 | PF00022 | 0.261 |
LIG_BRCT_BRCA1_1 | 255 | 259 | PF00533 | 0.411 |
LIG_BRCT_BRCA1_1 | 293 | 297 | PF00533 | 0.416 |
LIG_FHA_1 | 149 | 155 | PF00498 | 0.588 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.776 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.314 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.682 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.624 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.685 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.751 |
LIG_IRF3_LxIS_1 | 224 | 229 | PF10401 | 0.261 |
LIG_LIR_Gen_1 | 155 | 164 | PF02991 | 0.618 |
LIG_LIR_Gen_1 | 256 | 266 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 97 | 107 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 155 | 159 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 97 | 102 | PF02991 | 0.735 |
LIG_Pex14_1 | 344 | 348 | PF04695 | 0.396 |
LIG_Pex14_2 | 304 | 308 | PF04695 | 0.407 |
LIG_SH2_GRB2like | 248 | 251 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.394 |
LIG_SH3_3 | 157 | 163 | PF00018 | 0.638 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.261 |
LIG_SH3_3 | 306 | 312 | PF00018 | 0.509 |
LIG_SxIP_EBH_1 | 103 | 117 | PF03271 | 0.646 |
LIG_TRAF2_1 | 73 | 76 | PF00917 | 0.652 |
MOD_CDC14_SPxK_1 | 132 | 135 | PF00782 | 0.834 |
MOD_CDK_SPK_2 | 129 | 134 | PF00069 | 0.656 |
MOD_CDK_SPK_2 | 37 | 42 | PF00069 | 0.640 |
MOD_CDK_SPxK_1 | 129 | 135 | PF00069 | 0.837 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.842 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.651 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.568 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.411 |
MOD_CK1_1 | 356 | 362 | PF00069 | 0.593 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.717 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.749 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.603 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.613 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.558 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.556 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.472 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.710 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.479 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.491 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.547 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.483 |
MOD_GlcNHglycan | 90 | 94 | PF01048 | 0.429 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.729 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.792 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.625 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.636 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.355 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.444 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.745 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.678 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.762 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.665 |
MOD_N-GLC_1 | 360 | 365 | PF02516 | 0.652 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.803 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.388 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.609 |
MOD_NEK2_1 | 336 | 341 | PF00069 | 0.428 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.677 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.713 |
MOD_NEK2_2 | 98 | 103 | PF00069 | 0.707 |
MOD_PIKK_1 | 20 | 26 | PF00454 | 0.779 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.656 |
MOD_PKA_2 | 105 | 111 | PF00069 | 0.754 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.665 |
MOD_PKA_2 | 286 | 292 | PF00069 | 0.628 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.777 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.685 |
MOD_PKA_2 | 67 | 73 | PF00069 | 0.823 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.613 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.499 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.408 |
MOD_Plk_4 | 293 | 299 | PF00069 | 0.408 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.660 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.734 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.756 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.261 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.750 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.736 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.778 |
TRG_DiLeu_BaEn_1 | 189 | 194 | PF01217 | 0.610 |
TRG_DiLeu_BaEn_1 | 273 | 278 | PF01217 | 0.720 |
TRG_ER_diArg_1 | 266 | 269 | PF00400 | 0.667 |
TRG_ER_diArg_1 | 281 | 284 | PF00400 | 0.648 |
TRG_NLS_MonoExtC_3 | 102 | 107 | PF00514 | 0.633 |
TRG_Pf-PMV_PEXEL_1 | 191 | 196 | PF00026 | 0.471 |
TRG_Pf-PMV_PEXEL_1 | 275 | 280 | PF00026 | 0.522 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HV70 | Leptomonas seymouri | 48% | 100% |
A0A3Q8ID58 | Leishmania donovani | 77% | 100% |
A4I102 | Leishmania infantum | 77% | 100% |
E9AX40 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q4QAD6 | Leishmania major | 75% | 100% |