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: E9AMG0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.670 |
CLV_C14_Caspase3-7 | 157 | 161 | PF00656 | 0.599 |
CLV_C14_Caspase3-7 | 177 | 181 | PF00656 | 0.665 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.780 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.663 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.756 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.485 |
DOC_MAPK_gen_1 | 101 | 109 | PF00069 | 0.641 |
DOC_PP4_FxxP_1 | 205 | 208 | PF00568 | 0.567 |
DOC_PP4_MxPP_1 | 199 | 202 | PF00568 | 0.691 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.771 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.521 |
DOC_USP7_UBL2_3 | 133 | 137 | PF12436 | 0.645 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.564 |
LIG_AP2alpha_1 | 205 | 209 | PF02296 | 0.712 |
LIG_AP2alpha_2 | 187 | 189 | PF02296 | 0.679 |
LIG_AP2alpha_2 | 207 | 209 | PF02296 | 0.485 |
LIG_AP2alpha_2 | 284 | 286 | PF02296 | 0.482 |
LIG_BRCT_BRCA1_1 | 80 | 84 | PF00533 | 0.499 |
LIG_deltaCOP1_diTrp_1 | 183 | 189 | PF00928 | 0.640 |
LIG_EVH1_2 | 201 | 205 | PF00568 | 0.698 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.524 |
LIG_FHA_2 | 62 | 68 | PF00498 | 0.436 |
LIG_LIR_Apic_2 | 183 | 188 | PF02991 | 0.723 |
LIG_LIR_Gen_1 | 284 | 290 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 81 | 87 | PF02991 | 0.478 |
LIG_Pex14_2 | 205 | 209 | PF04695 | 0.712 |
LIG_Pex14_2 | 248 | 252 | PF04695 | 0.503 |
LIG_SH2_GRB2like | 56 | 59 | PF00017 | 0.449 |
LIG_SH2_NCK_1 | 158 | 162 | PF00017 | 0.671 |
LIG_SH2_STAP1 | 53 | 57 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.548 |
LIG_SH3_2 | 258 | 263 | PF14604 | 0.561 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.636 |
LIG_SH3_3 | 176 | 182 | PF00018 | 0.524 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.560 |
LIG_SUMO_SIM_par_1 | 105 | 111 | PF11976 | 0.707 |
LIG_TRAF2_1 | 64 | 67 | PF00917 | 0.461 |
MOD_CDC14_SPxK_1 | 260 | 263 | PF00782 | 0.543 |
MOD_CDK_SPxK_1 | 257 | 263 | PF00069 | 0.563 |
MOD_CDK_SPxxK_3 | 22 | 29 | PF00069 | 0.608 |
MOD_CDK_SPxxK_3 | 233 | 240 | PF00069 | 0.654 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.717 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.600 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.581 |
MOD_CK2_1 | 61 | 67 | PF00069 | 0.426 |
MOD_Cter_Amidation | 169 | 172 | PF01082 | 0.734 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.676 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.772 |
MOD_GlcNHglycan | 21 | 25 | PF01048 | 0.572 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.653 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.581 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.503 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.590 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.739 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.685 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.511 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.487 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.565 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.646 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.487 |
MOD_PKA_1 | 6 | 12 | PF00069 | 0.655 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.683 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.604 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.663 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.564 |
MOD_Plk_2-3 | 61 | 67 | PF00069 | 0.426 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.638 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.468 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.612 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.624 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.599 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.568 |
TRG_ER_diArg_1 | 103 | 106 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 29 | 31 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.660 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEG2 | Leptomonas seymouri | 39% | 100% |
A0A3S5H670 | Leishmania donovani | 84% | 100% |
A4H6C7 | Leishmania braziliensis | 59% | 100% |
A4HTM6 | Leishmania infantum | 84% | 100% |
Q4QI83 | Leishmania major | 81% | 100% |