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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4QHA9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.436 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.349 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.374 |
CLV_PCSK_PC7_1 | 230 | 236 | PF00082 | 0.677 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.581 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.324 |
DEG_APCC_KENBOX_2 | 196 | 200 | PF00400 | 0.566 |
DOC_ANK_TNKS_1 | 33 | 40 | PF00023 | 0.486 |
DOC_CKS1_1 | 47 | 52 | PF01111 | 0.246 |
DOC_CYCLIN_RxL_1 | 40 | 49 | PF00134 | 0.246 |
DOC_CYCLIN_RxL_1 | 92 | 99 | PF00134 | 0.402 |
DOC_MAPK_gen_1 | 58 | 64 | PF00069 | 0.368 |
DOC_MIT_MIM_1 | 56 | 64 | PF04212 | 0.434 |
DOC_PP1_RVXF_1 | 41 | 48 | PF00149 | 0.430 |
DOC_PP4_FxxP_1 | 141 | 144 | PF00568 | 0.582 |
DOC_PP4_FxxP_1 | 153 | 156 | PF00568 | 0.553 |
DOC_PP4_FxxP_1 | 47 | 50 | PF00568 | 0.335 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.782 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.535 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.246 |
LIG_14-3-3_CanoR_1 | 151 | 156 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 159 | 166 | PF00244 | 0.554 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.452 |
LIG_deltaCOP1_diTrp_1 | 131 | 141 | PF00928 | 0.651 |
LIG_LIR_Apic_2 | 140 | 144 | PF02991 | 0.582 |
LIG_LIR_Gen_1 | 131 | 141 | PF02991 | 0.684 |
LIG_LIR_Gen_1 | 179 | 187 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 216 | 227 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 88 | 98 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 131 | 137 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 179 | 183 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 88 | 94 | PF02991 | 0.335 |
LIG_MAD2 | 43 | 51 | PF02301 | 0.363 |
LIG_MLH1_MIPbox_1 | 215 | 219 | PF16413 | 0.522 |
LIG_NRBOX | 93 | 99 | PF00104 | 0.408 |
LIG_Pex14_2 | 153 | 157 | PF04695 | 0.604 |
LIG_SH2_CRK | 91 | 95 | PF00017 | 0.335 |
LIG_SH2_NCK_1 | 12 | 16 | PF00017 | 0.421 |
LIG_SH2_PTP2 | 271 | 274 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 186 | 190 | PF00017 | 0.579 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.480 |
LIG_TYR_ITIM | 10 | 15 | PF00017 | 0.415 |
LIG_TYR_ITIM | 269 | 274 | PF00017 | 0.498 |
MOD_CDK_SPK_2 | 258 | 263 | PF00069 | 0.388 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.698 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.638 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.378 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.481 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.576 |
MOD_Cter_Amidation | 250 | 253 | PF01082 | 0.500 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.690 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.695 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.661 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.538 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.655 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.612 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.526 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.637 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.586 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.372 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.471 |
MOD_N-GLC_1 | 176 | 181 | PF02516 | 0.525 |
MOD_NEK2_2 | 265 | 270 | PF00069 | 0.600 |
MOD_NMyristoyl | 1 | 7 | PF02799 | 0.417 |
MOD_PKA_1 | 229 | 235 | PF00069 | 0.699 |
MOD_PKA_2 | 112 | 118 | PF00069 | 0.744 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.620 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.587 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.699 |
MOD_PKB_1 | 111 | 119 | PF00069 | 0.633 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.448 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.637 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.390 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.246 |
MOD_SUMO_rev_2 | 164 | 174 | PF00179 | 0.584 |
MOD_SUMO_rev_2 | 71 | 80 | PF00179 | 0.363 |
TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.669 |
TRG_ENDOCYTIC_2 | 271 | 274 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 110 | 113 | PF00400 | 0.593 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 252 | 255 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 57 | 60 | PF00400 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 188 | 193 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 43 | 48 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 95 | 99 | PF00026 | 0.410 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRV7 | Leptomonas seymouri | 57% | 100% |
A0A0S4JQU3 | Bodo saltans | 31% | 100% |
A0A1X0NRW0 | Trypanosomatidae | 34% | 100% |
A0A3Q8IB40 | Leishmania donovani | 88% | 100% |
A0A3R7ND09 | Trypanosoma rangeli | 34% | 100% |
A4H693 | Leishmania braziliensis | 76% | 100% |
A4HUL6 | Leishmania infantum | 89% | 100% |
C9ZVP3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9ANB5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |