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 |
Related structures:
AlphaFold database: E9B4T6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.721 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.532 |
DEG_SPOP_SBC_1 | 120 | 124 | PF00917 | 0.548 |
DOC_CYCLIN_yCln2_LP_2 | 198 | 204 | PF00134 | 0.587 |
DOC_MAPK_HePTP_8 | 84 | 96 | PF00069 | 0.552 |
DOC_MAPK_MEF2A_6 | 245 | 254 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 78 | 86 | PF00069 | 0.560 |
DOC_MAPK_MEF2A_6 | 87 | 96 | PF00069 | 0.525 |
DOC_PP2B_LxvP_1 | 178 | 181 | PF13499 | 0.577 |
DOC_PP2B_PxIxI_1 | 91 | 97 | PF00149 | 0.536 |
DOC_PP4_FxxP_1 | 23 | 26 | PF00568 | 0.500 |
DOC_PP4_FxxP_1 | 68 | 71 | PF00568 | 0.572 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.472 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.711 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.587 |
DOC_WW_Pin1_4 | 203 | 208 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.580 |
LIG_14-3-3_CanoR_1 | 118 | 127 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 168 | 178 | PF00244 | 0.616 |
LIG_14-3-3_CanoR_1 | 195 | 199 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 263 | 272 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 281 | 290 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 291 | 297 | PF00244 | 0.581 |
LIG_14-3-3_CanoR_1 | 47 | 52 | PF00244 | 0.569 |
LIG_14-3-3_CanoR_1 | 7 | 13 | PF00244 | 0.577 |
LIG_14-3-3_CterR_2 | 377 | 379 | PF00244 | 0.583 |
LIG_Actin_WH2_2 | 181 | 197 | PF00022 | 0.642 |
LIG_Actin_WH2_2 | 334 | 349 | PF00022 | 0.475 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.622 |
LIG_BIR_III_2 | 39 | 43 | PF00653 | 0.584 |
LIG_BRCT_BRCA1_1 | 123 | 127 | PF00533 | 0.540 |
LIG_deltaCOP1_diTrp_1 | 274 | 277 | PF00928 | 0.486 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.551 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.665 |
LIG_FHA_1 | 71 | 77 | PF00498 | 0.685 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.536 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.509 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.552 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.569 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.502 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.549 |
LIG_LIR_Apic_2 | 20 | 26 | PF02991 | 0.504 |
LIG_LIR_Apic_2 | 274 | 278 | PF02991 | 0.491 |
LIG_LIR_Apic_2 | 65 | 71 | PF02991 | 0.565 |
LIG_LIR_Gen_1 | 356 | 366 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.553 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 274 | 280 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 356 | 361 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.588 |
LIG_Pex14_2 | 34 | 38 | PF04695 | 0.606 |
LIG_SH2_CRK | 98 | 102 | PF00017 | 0.549 |
LIG_SH3_2 | 204 | 209 | PF14604 | 0.572 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.571 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.605 |
LIG_SH3_3 | 329 | 335 | PF00018 | 0.594 |
LIG_SUMO_SIM_anti_2 | 328 | 334 | PF11976 | 0.603 |
LIG_SUMO_SIM_par_1 | 140 | 149 | PF11976 | 0.585 |
LIG_TYR_ITIM | 96 | 101 | PF00017 | 0.517 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.563 |
LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.539 |
MOD_CDC14_SPxK_1 | 206 | 209 | PF00782 | 0.576 |
MOD_CDK_SPxK_1 | 203 | 209 | PF00069 | 0.570 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.550 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.699 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.760 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.586 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.586 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.575 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.587 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.507 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.603 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.531 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.630 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.492 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.523 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.526 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.545 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.552 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.736 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.705 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.583 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.618 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.521 |
MOD_GlcNHglycan | 43 | 47 | PF01048 | 0.665 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.531 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.543 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.551 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.577 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.645 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.560 |
MOD_GSK3_1 | 255 | 262 | PF00069 | 0.503 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.584 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.521 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.564 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.550 |
MOD_N-GLC_1 | 13 | 18 | PF02516 | 0.613 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.598 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.547 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.488 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.461 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.540 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.528 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.567 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.654 |
MOD_PIKK_1 | 70 | 76 | PF00454 | 0.661 |
MOD_PKA_2 | 170 | 176 | PF00069 | 0.632 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.487 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.478 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.509 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.532 |
MOD_Plk_1 | 19 | 25 | PF00069 | 0.625 |
MOD_Plk_1 | 259 | 265 | PF00069 | 0.596 |
MOD_Plk_1 | 327 | 333 | PF00069 | 0.617 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.620 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.617 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.587 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.564 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.577 |
TRG_DiLeu_BaEn_1 | 104 | 109 | PF01217 | 0.532 |
TRG_DiLeu_BaLyEn_6 | 252 | 257 | PF01217 | 0.505 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.554 |
TRG_ER_diArg_1 | 288 | 291 | PF00400 | 0.588 |
TRG_NES_CRM1_1 | 74 | 88 | PF08389 | 0.555 |
TRG_Pf-PMV_PEXEL_1 | 255 | 260 | PF00026 | 0.577 |
TRG_Pf-PMV_PEXEL_1 | 270 | 274 | PF00026 | 0.406 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HWJ1 | Leptomonas seymouri | 52% | 78% |
A0A3Q8IH36 | Leishmania donovani | 91% | 98% |
A4HAN3 | Leishmania braziliensis | 78% | 100% |
A4I9S5 | Leishmania infantum | 92% | 98% |
Q4Q390 | Leishmania major | 92% | 100% |