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: A0A3S7XB07
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.602 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 296 | 300 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 61 | 65 | PF00082 | 0.559 |
DEG_APCC_DBOX_1 | 201 | 209 | PF00400 | 0.475 |
DOC_CYCLIN_RxL_1 | 199 | 206 | PF00134 | 0.468 |
DOC_CYCLIN_RxL_1 | 290 | 302 | PF00134 | 0.546 |
DOC_CYCLIN_RxL_1 | 339 | 348 | PF00134 | 0.593 |
DOC_CYCLIN_yCln2_LP_2 | 187 | 193 | PF00134 | 0.673 |
DOC_CYCLIN_yCln2_LP_2 | 59 | 65 | PF00134 | 0.502 |
DOC_MAPK_DCC_7 | 188 | 198 | PF00069 | 0.626 |
DOC_MAPK_gen_1 | 88 | 97 | PF00069 | 0.366 |
DOC_MAPK_MEF2A_6 | 91 | 99 | PF00069 | 0.362 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.692 |
DOC_PP2B_LxvP_1 | 79 | 82 | PF13499 | 0.404 |
DOC_PP4_FxxP_1 | 28 | 31 | PF00568 | 0.485 |
DOC_PP4_FxxP_1 | 325 | 328 | PF00568 | 0.529 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.428 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 237 | 242 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 289 | 294 | PF00397 | 0.666 |
LIG_14-3-3_CanoR_1 | 88 | 94 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 9 | 17 | PF00244 | 0.405 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.475 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.534 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.510 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.419 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.358 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.549 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.516 |
LIG_LIR_Apic_2 | 322 | 328 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 16 | 25 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 327 | 337 | PF02991 | 0.505 |
LIG_LIR_Gen_1 | 37 | 45 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 75 | 86 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 16 | 20 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 327 | 333 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.569 |
LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 92 | 96 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 98 | 102 | PF02991 | 0.431 |
LIG_NRP_CendR_1 | 349 | 350 | PF00754 | 0.634 |
LIG_Pex14_2 | 24 | 28 | PF04695 | 0.457 |
LIG_Pex14_2 | 39 | 43 | PF04695 | 0.392 |
LIG_SH2_CRK | 17 | 21 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 17 | 21 | PF00017 | 0.419 |
LIG_SH2_STAT3 | 102 | 105 | PF00017 | 0.423 |
LIG_SH2_STAT3 | 266 | 269 | PF00017 | 0.594 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.522 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.391 |
LIG_SH3_1 | 108 | 114 | PF00018 | 0.614 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.614 |
LIG_SH3_3 | 119 | 125 | PF00018 | 0.502 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.648 |
LIG_SH3_3 | 187 | 193 | PF00018 | 0.590 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.502 |
LIG_SUMO_SIM_par_1 | 194 | 199 | PF11976 | 0.502 |
LIG_SUMO_SIM_par_1 | 68 | 76 | PF11976 | 0.464 |
LIG_TRAF2_1 | 314 | 317 | PF00917 | 0.706 |
LIG_WRC_WIRS_1 | 96 | 101 | PF05994 | 0.419 |
MOD_CDK_SPxxK_3 | 289 | 296 | PF00069 | 0.587 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.603 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.600 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.643 |
MOD_CK2_1 | 129 | 135 | PF00069 | 0.654 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.657 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.490 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.607 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.476 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.418 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.524 |
MOD_CK2_1 | 77 | 83 | PF00069 | 0.403 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.656 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.750 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.557 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.598 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.728 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.452 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.403 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.598 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.405 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.684 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.609 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.602 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.805 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.588 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.480 |
MOD_GSK3_1 | 73 | 80 | PF00069 | 0.494 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.583 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.695 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.609 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.515 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.515 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.570 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.435 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.370 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.388 |
MOD_NEK2_2 | 320 | 325 | PF00069 | 0.517 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.437 |
MOD_PIKK_1 | 158 | 164 | PF00454 | 0.632 |
MOD_PKA_1 | 256 | 262 | PF00069 | 0.550 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.490 |
MOD_PKA_2 | 256 | 262 | PF00069 | 0.562 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.509 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.620 |
MOD_Plk_1 | 43 | 49 | PF00069 | 0.491 |
MOD_Plk_2-3 | 32 | 38 | PF00069 | 0.423 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.629 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.577 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.370 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.630 |
MOD_ProDKin_1 | 237 | 243 | PF00069 | 0.650 |
MOD_ProDKin_1 | 289 | 295 | PF00069 | 0.664 |
MOD_SUMO_rev_2 | 245 | 252 | PF00179 | 0.530 |
TRG_DiLeu_BaLyEn_6 | 199 | 204 | PF01217 | 0.539 |
TRG_DiLeu_BaLyEn_6 | 340 | 345 | PF01217 | 0.597 |
TRG_ENDOCYTIC_2 | 17 | 20 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.494 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.666 |
TRG_ER_diArg_1 | 331 | 334 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.592 |
TRG_NES_CRM1_1 | 19 | 32 | PF08389 | 0.464 |
TRG_Pf-PMV_PEXEL_1 | 343 | 348 | PF00026 | 0.600 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5Y4 | Leptomonas seymouri | 48% | 100% |
A4HPB8 | Leishmania braziliensis | 81% | 100% |
A4ICF8 | Leishmania infantum | 99% | 100% |
E9AT29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4Q1G9 | Leishmania major | 92% | 100% |