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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9AGD7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.611 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.611 |
DOC_MAPK_gen_1 | 39 | 47 | PF00069 | 0.604 |
DOC_PP2B_LxvP_1 | 29 | 32 | PF13499 | 0.695 |
DOC_PP4_FxxP_1 | 74 | 77 | PF00568 | 0.729 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 155 | 159 | PF00917 | 0.686 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 32 | 36 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.590 |
DOC_USP7_MATH_2 | 165 | 171 | PF00917 | 0.715 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.676 |
LIG_14-3-3_CanoR_1 | 11 | 19 | PF00244 | 0.606 |
LIG_deltaCOP1_diTrp_1 | 214 | 223 | PF00928 | 0.622 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.633 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.610 |
LIG_FHA_2 | 265 | 271 | PF00498 | 0.680 |
LIG_LIR_Apic_2 | 60 | 65 | PF02991 | 0.684 |
LIG_LIR_LC3C_4 | 42 | 46 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 237 | 241 | PF02991 | 0.697 |
LIG_Pex14_1 | 182 | 186 | PF04695 | 0.640 |
LIG_SH2_CRK | 62 | 66 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.643 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.664 |
LIG_SH3_3 | 74 | 80 | PF00018 | 0.778 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.733 |
LIG_SUMO_SIM_anti_2 | 42 | 48 | PF11976 | 0.647 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.701 |
LIG_TRAF2_1 | 296 | 299 | PF00917 | 0.640 |
MOD_CDK_SPK_2 | 226 | 231 | PF00069 | 0.676 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.766 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.633 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.678 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.543 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.673 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.733 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.630 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.678 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.595 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.600 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.748 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.666 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.744 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.693 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.658 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.667 |
MOD_GlcNHglycan | 224 | 228 | PF01048 | 0.502 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.763 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.645 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.689 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.589 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.747 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.717 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.626 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.774 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.683 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.683 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.675 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.704 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.598 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.666 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.594 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.562 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.657 |
MOD_N-GLC_1 | 202 | 207 | PF02516 | 0.602 |
MOD_N-GLC_1 | 83 | 88 | PF02516 | 0.696 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.774 |
MOD_NEK2_1 | 12 | 17 | PF00069 | 0.586 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.642 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.670 |
MOD_PIKK_1 | 187 | 193 | PF00454 | 0.613 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.650 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.713 |
MOD_Plk_4 | 157 | 163 | PF00069 | 0.628 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.653 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.671 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.678 |
MOD_SUMO_rev_2 | 88 | 98 | PF00179 | 0.694 |
TRG_DiLeu_BaLyEn_6 | 68 | 73 | PF01217 | 0.699 |
TRG_ER_diArg_1 | 39 | 41 | PF00400 | 0.622 |
TRG_Pf-PMV_PEXEL_1 | 175 | 179 | PF00026 | 0.671 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8I979 | Leishmania donovani | 99% | 100% |
A4H6W8 | Leishmania braziliensis | 69% | 100% |
E9ANX7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QGP3 | Leishmania major | 92% | 100% |