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: A4H5V6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 265 | 269 | PF00656 | 0.554 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.583 |
CLV_NRD_NRD_1 | 311 | 313 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.520 |
CLV_PCSK_KEX2_1 | 311 | 313 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 321 | 323 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.779 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.574 |
CLV_Separin_Metazoa | 112 | 116 | PF03568 | 0.549 |
DEG_APCC_KENBOX_2 | 351 | 355 | PF00400 | 0.366 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.553 |
DEG_SCF_FBW7_2 | 222 | 228 | PF00400 | 0.656 |
DOC_CKS1_1 | 222 | 227 | PF01111 | 0.599 |
DOC_CYCLIN_RxL_1 | 318 | 327 | PF00134 | 0.529 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 233 | 239 | PF00134 | 0.508 |
DOC_MAPK_gen_1 | 318 | 326 | PF00069 | 0.629 |
DOC_MAPK_gen_1 | 337 | 346 | PF00069 | 0.336 |
DOC_MAPK_gen_1 | 45 | 53 | PF00069 | 0.540 |
DOC_PP1_RVXF_1 | 170 | 177 | PF00149 | 0.517 |
DOC_PP2B_LxvP_1 | 143 | 146 | PF13499 | 0.521 |
DOC_USP7_MATH_1 | 106 | 110 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 273 | 277 | PF00917 | 0.591 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.669 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.627 |
LIG_14-3-3_CanoR_1 | 171 | 177 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 292 | 301 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 6 | 10 | PF00244 | 0.717 |
LIG_14-3-3_CanoR_1 | 95 | 99 | PF00244 | 0.608 |
LIG_BIR_III_4 | 327 | 331 | PF00653 | 0.446 |
LIG_BRCT_BRCA1_1 | 222 | 226 | PF00533 | 0.542 |
LIG_Clathr_ClatBox_1 | 323 | 327 | PF01394 | 0.529 |
LIG_Clathr_ClatBox_1 | 332 | 336 | PF01394 | 0.543 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.589 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.784 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.551 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.527 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.581 |
LIG_SH2_STAT3 | 243 | 246 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.678 |
LIG_SH2_STAT5 | 315 | 318 | PF00017 | 0.507 |
LIG_SH3_1 | 298 | 304 | PF00018 | 0.532 |
LIG_SH3_3 | 151 | 157 | PF00018 | 0.566 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.635 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.532 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.532 |
LIG_SUMO_SIM_anti_2 | 150 | 156 | PF11976 | 0.523 |
LIG_SUMO_SIM_anti_2 | 5 | 13 | PF11976 | 0.541 |
LIG_SUMO_SIM_par_1 | 122 | 130 | PF11976 | 0.538 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.631 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.779 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.664 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.598 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.795 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.516 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.582 |
MOD_Cter_Amidation | 319 | 322 | PF01082 | 0.626 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.676 |
MOD_GlcNHglycan | 130 | 134 | PF01048 | 0.627 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.677 |
MOD_GlcNHglycan | 148 | 152 | PF01048 | 0.649 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.548 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.506 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.363 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.637 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.616 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.607 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.470 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.506 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.713 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.707 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.702 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.588 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.646 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.718 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.450 |
MOD_N-GLC_1 | 215 | 220 | PF02516 | 0.376 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.364 |
MOD_N-GLC_1 | 93 | 98 | PF02516 | 0.710 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.530 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.486 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.776 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.610 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.798 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.658 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.795 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.748 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.608 |
MOD_PKA_2 | 79 | 85 | PF00069 | 0.766 |
MOD_PKA_2 | 94 | 100 | PF00069 | 0.696 |
MOD_Plk_1 | 147 | 153 | PF00069 | 0.577 |
MOD_Plk_1 | 172 | 178 | PF00069 | 0.442 |
MOD_Plk_1 | 215 | 221 | PF00069 | 0.381 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.650 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.674 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.686 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.617 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.627 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.440 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.517 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.628 |
TRG_DiLeu_BaLyEn_6 | 319 | 324 | PF01217 | 0.526 |
TRG_ENDOCYTIC_2 | 183 | 186 | PF00928 | 0.460 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.721 |
TRG_ER_diArg_1 | 321 | 323 | PF00400 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 322 | 327 | PF00026 | 0.528 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDM6 | Leptomonas seymouri | 47% | 98% |
A0A3Q8IBZ5 | Leishmania donovani | 63% | 100% |
A4HU50 | Leishmania infantum | 63% | 100% |
E9AMX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 100% |
Q4QHP7 | Leishmania major | 64% | 100% |