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 | yes | yes: 1, no: 4 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: A4HHY6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 233 | 235 | PF00675 | 0.457 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 229 | 231 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 2 | 4 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.645 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.433 |
DOC_CKS1_1 | 63 | 68 | PF01111 | 0.418 |
DOC_PP4_FxxP_1 | 199 | 202 | PF00568 | 0.711 |
DOC_SPAK_OSR1_1 | 83 | 87 | PF12202 | 0.243 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.394 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.726 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.465 |
LIG_14-3-3_CanoR_1 | 222 | 226 | PF00244 | 0.759 |
LIG_deltaCOP1_diTrp_1 | 74 | 84 | PF00928 | 0.441 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.703 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.745 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.629 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.703 |
LIG_LIR_Apic_2 | 197 | 202 | PF02991 | 0.711 |
LIG_LIR_Apic_2 | 32 | 38 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 175 | 186 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 110 | 114 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 74 | 80 | PF02991 | 0.509 |
LIG_LIR_Nem_3 | 81 | 87 | PF02991 | 0.374 |
LIG_Pex14_2 | 84 | 88 | PF04695 | 0.442 |
LIG_Rb_LxCxE_1 | 165 | 188 | PF01857 | 0.616 |
LIG_SH2_CRK | 233 | 237 | PF00017 | 0.604 |
LIG_SH2_CRK | 35 | 39 | PF00017 | 0.404 |
LIG_SH2_SRC | 59 | 62 | PF00017 | 0.436 |
LIG_SH2_STAT3 | 39 | 42 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.692 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.520 |
LIG_SUMO_SIM_par_1 | 19 | 25 | PF11976 | 0.453 |
MOD_CDK_SPxxK_3 | 62 | 69 | PF00069 | 0.420 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.697 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.660 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.593 |
MOD_CK1_1 | 159 | 165 | PF00069 | 0.630 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.722 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.631 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.669 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.484 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.440 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.724 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.693 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.630 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.703 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.516 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.596 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.661 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.687 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.657 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.686 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.712 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.684 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.542 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.799 |
MOD_N-GLC_1 | 192 | 197 | PF02516 | 0.520 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.631 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.683 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.672 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.375 |
MOD_NEK2_2 | 78 | 83 | PF00069 | 0.392 |
MOD_PIKK_1 | 187 | 193 | PF00454 | 0.711 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.623 |
MOD_PIKK_1 | 238 | 244 | PF00454 | 0.613 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.703 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.530 |
MOD_Plk_2-3 | 140 | 146 | PF00069 | 0.680 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.406 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.405 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.686 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.726 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.529 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.463 |
TRG_DiLeu_BaEn_2 | 173 | 179 | PF01217 | 0.607 |
TRG_DiLeu_BaEn_4 | 176 | 182 | PF01217 | 0.677 |
TRG_ENDOCYTIC_2 | 111 | 114 | PF00928 | 0.667 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.602 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X330 | Leishmania donovani | 64% | 98% |
A4I566 | Leishmania infantum | 64% | 98% |
E9B0G3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 92% |
Q4Q7S0 | Leishmania major | 55% | 100% |