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: A4I0I3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.632 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.572 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.770 |
CLV_NRD_NRD_1 | 94 | 96 | PF00675 | 0.642 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 38 | 40 | PF00082 | 0.710 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.639 |
CLV_PCSK_PC1ET2_1 | 38 | 40 | PF00082 | 0.710 |
CLV_PCSK_PC1ET2_1 | 93 | 95 | PF00082 | 0.678 |
CLV_PCSK_PC7_1 | 34 | 40 | PF00082 | 0.708 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.753 |
DEG_SPOP_SBC_1 | 16 | 20 | PF00917 | 0.768 |
DEG_SPOP_SBC_1 | 192 | 196 | PF00917 | 0.746 |
DOC_CYCLIN_RxL_1 | 155 | 164 | PF00134 | 0.671 |
DOC_CYCLIN_RxL_1 | 93 | 105 | PF00134 | 0.642 |
DOC_MAPK_gen_1 | 93 | 101 | PF00069 | 0.615 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.738 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.768 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.717 |
DOC_USP7_UBL2_3 | 93 | 97 | PF12436 | 0.578 |
LIG_14-3-3_CanoR_1 | 12 | 17 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 158 | 163 | PF00244 | 0.587 |
LIG_14-3-3_CanoR_1 | 178 | 184 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 49 | 55 | PF00244 | 0.742 |
LIG_14-3-3_CanoR_1 | 94 | 100 | PF00244 | 0.594 |
LIG_BRCT_BRCA1_1 | 103 | 107 | PF00533 | 0.735 |
LIG_Clathr_ClatBox_1 | 159 | 163 | PF01394 | 0.579 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.635 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.627 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.596 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.574 |
LIG_FHA_2 | 224 | 230 | PF00498 | 0.620 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.628 |
LIG_Pex14_2 | 107 | 111 | PF04695 | 0.638 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.669 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.663 |
LIG_SH3_2 | 213 | 218 | PF14604 | 0.758 |
LIG_SH3_2 | 80 | 85 | PF14604 | 0.749 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.739 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.753 |
LIG_SUMO_SIM_par_1 | 158 | 164 | PF11976 | 0.681 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.552 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.753 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.722 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.790 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.643 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.682 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.682 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.656 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.580 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.642 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.677 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.639 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.591 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.732 |
MOD_GlcNHglycan | 204 | 208 | PF01048 | 0.740 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.752 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.726 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.737 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.662 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.720 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.711 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.679 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.784 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.707 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.608 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.700 |
MOD_PIKK_1 | 20 | 26 | PF00454 | 0.594 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.707 |
MOD_PK_1 | 12 | 18 | PF00069 | 0.765 |
MOD_PKA_1 | 49 | 55 | PF00069 | 0.598 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.744 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.627 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.618 |
MOD_SUMO_for_1 | 37 | 40 | PF00179 | 0.709 |
TRG_DiLeu_BaLyEn_6 | 155 | 160 | PF01217 | 0.667 |
TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.730 |
TRG_ER_diArg_1 | 238 | 240 | PF00400 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 158 | 163 | PF00026 | 0.576 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4W9 | Leptomonas seymouri | 51% | 100% |
A0A3S7WXU2 | Leishmania donovani | 99% | 100% |
A4HCZ8 | Leishmania braziliensis | 70% | 100% |
E9AWE5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4QB27 | Leishmania major | 91% | 100% |