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: Q4QI83
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 150 | 154 | PF00656 | 0.692 |
CLV_C14_Caspase3-7 | 157 | 161 | PF00656 | 0.580 |
CLV_C14_Caspase3-7 | 177 | 181 | PF00656 | 0.677 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.703 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 214 | 216 | PF00675 | 0.732 |
CLV_NRD_NRD_1 | 220 | 222 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.702 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 214 | 216 | PF00082 | 0.732 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.699 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.701 |
CLV_PCSK_PC1ET2_1 | 139 | 141 | PF00082 | 0.699 |
CLV_PCSK_SKI1_1 | 220 | 224 | PF00082 | 0.616 |
DOC_MAPK_gen_1 | 101 | 109 | PF00069 | 0.681 |
DOC_PP4_MxPP_1 | 199 | 202 | PF00568 | 0.733 |
DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 225 | 229 | PF00917 | 0.592 |
DOC_USP7_UBL2_3 | 133 | 137 | PF12436 | 0.690 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 221 | 226 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.701 |
DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 257 | 262 | PF00397 | 0.601 |
LIG_14-3-3_CanoR_1 | 140 | 148 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 7 | 16 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 95 | 100 | PF00244 | 0.544 |
LIG_AP2alpha_1 | 205 | 209 | PF02296 | 0.764 |
LIG_AP2alpha_2 | 187 | 189 | PF02296 | 0.725 |
LIG_AP2alpha_2 | 284 | 286 | PF02296 | 0.501 |
LIG_BIR_III_2 | 207 | 211 | PF00653 | 0.653 |
LIG_BRCT_BRCA1_1 | 244 | 248 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_1 | 80 | 84 | PF00533 | 0.521 |
LIG_deltaCOP1_diTrp_1 | 183 | 189 | PF00928 | 0.669 |
LIG_EVH1_2 | 201 | 205 | PF00568 | 0.744 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.492 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.573 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.506 |
LIG_LIR_Apic_2 | 183 | 188 | PF02991 | 0.726 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 81 | 87 | PF02991 | 0.498 |
LIG_Pex14_2 | 205 | 209 | PF04695 | 0.764 |
LIG_Pex14_2 | 65 | 69 | PF04695 | 0.633 |
LIG_SH2_GRB2like | 56 | 59 | PF00017 | 0.483 |
LIG_SH2_NCK_1 | 158 | 162 | PF00017 | 0.700 |
LIG_SH2_STAP1 | 53 | 57 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.583 |
LIG_SH3_2 | 258 | 263 | PF14604 | 0.600 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.728 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.643 |
LIG_SH3_3 | 255 | 261 | PF00018 | 0.567 |
LIG_SUMO_SIM_par_1 | 105 | 111 | PF11976 | 0.759 |
LIG_TRAF2_1 | 64 | 67 | PF00917 | 0.515 |
MOD_CDC14_SPxK_1 | 260 | 263 | PF00782 | 0.592 |
MOD_CDK_SPxK_1 | 257 | 263 | PF00069 | 0.598 |
MOD_CDK_SPxxK_3 | 22 | 29 | PF00069 | 0.647 |
MOD_CDK_SPxxK_3 | 233 | 240 | PF00069 | 0.699 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.691 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.774 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.636 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.427 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.593 |
MOD_Cter_Amidation | 169 | 172 | PF01082 | 0.772 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.722 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.605 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.639 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.750 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.523 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.544 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.585 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.514 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.565 |
MOD_N-GLC_1 | 95 | 100 | PF02516 | 0.579 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.652 |
MOD_NEK2_1 | 52 | 57 | PF00069 | 0.592 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.514 |
MOD_PK_1 | 223 | 229 | PF00069 | 0.564 |
MOD_PKA_1 | 139 | 145 | PF00069 | 0.684 |
MOD_PKA_1 | 6 | 12 | PF00069 | 0.693 |
MOD_PKA_2 | 139 | 145 | PF00069 | 0.699 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.471 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.637 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.498 |
MOD_PKB_1 | 45 | 53 | PF00069 | 0.455 |
MOD_Plk_1 | 95 | 101 | PF00069 | 0.578 |
MOD_Plk_2-3 | 151 | 157 | PF00069 | 0.551 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.702 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.496 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.538 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.543 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.653 |
MOD_ProDKin_1 | 221 | 227 | PF00069 | 0.628 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.697 |
MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.583 |
MOD_ProDKin_1 | 257 | 263 | PF00069 | 0.604 |
TRG_ER_diArg_1 | 103 | 106 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 166 | 168 | PF00400 | 0.583 |
TRG_ER_diArg_1 | 220 | 222 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.692 |
TRG_ER_diArg_1 | 5 | 7 | PF00400 | 0.701 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEG2 | Leptomonas seymouri | 39% | 100% |
A0A3S5H670 | Leishmania donovani | 87% | 100% |
A4H6C7 | Leishmania braziliensis | 58% | 91% |
A4HTM6 | Leishmania infantum | 87% | 100% |
E9AMG0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |