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: 3 |
NetGPI | no | yes: 0, no: 3 |
Related structures:
AlphaFold database: A4IDF1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.424 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.620 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 198 | 200 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.482 |
CLV_PCSK_PC7_1 | 9 | 15 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.415 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.394 |
DEG_APCC_DBOX_1 | 177 | 185 | PF00400 | 0.455 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.407 |
DOC_MAPK_gen_1 | 42 | 51 | PF00069 | 0.419 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.687 |
LIG_14-3-3_CanoR_1 | 230 | 236 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 27 | 37 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 42 | 46 | PF00244 | 0.334 |
LIG_APCC_ABBA_1 | 49 | 54 | PF00400 | 0.372 |
LIG_APCC_ABBAyCdc20_2 | 48 | 54 | PF00400 | 0.375 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.379 |
LIG_FHA_2 | 19 | 25 | PF00498 | 0.365 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.456 |
LIG_PDZ_Class_3 | 243 | 248 | PF00595 | 0.524 |
LIG_Pex14_2 | 41 | 45 | PF04695 | 0.347 |
LIG_SH2_NCK_1 | 213 | 217 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 52 | 56 | PF00017 | 0.372 |
LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.349 |
LIG_SH2_STAT3 | 109 | 112 | PF00017 | 0.458 |
LIG_SH3_3 | 238 | 244 | PF00018 | 0.487 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.437 |
LIG_TRAF2_1 | 78 | 81 | PF00917 | 0.423 |
LIG_UBA3_1 | 7 | 13 | PF00899 | 0.362 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.350 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.623 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.537 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.355 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.437 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.388 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.475 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.654 |
MOD_N-GLC_1 | 138 | 143 | PF02516 | 0.484 |
MOD_N-GLC_1 | 54 | 59 | PF02516 | 0.451 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.482 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.351 |
MOD_PIKK_1 | 229 | 235 | PF00454 | 0.428 |
MOD_PKA_1 | 13 | 19 | PF00069 | 0.348 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.348 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.423 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.386 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.360 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.414 |
MOD_Plk_1 | 54 | 60 | PF00069 | 0.447 |
MOD_Plk_2-3 | 18 | 24 | PF00069 | 0.355 |
MOD_SUMO_for_1 | 153 | 156 | PF00179 | 0.450 |
TRG_DiLeu_BaEn_1 | 32 | 37 | PF01217 | 0.396 |
TRG_DiLeu_BaEn_3 | 196 | 202 | PF01217 | 0.422 |
TRG_DiLeu_BaLyEn_6 | 6 | 11 | PF01217 | 0.444 |
TRG_DiLeu_LyEn_5 | 32 | 37 | PF01217 | 0.396 |
TRG_ER_diArg_1 | 198 | 200 | PF00400 | 0.424 |