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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005789 | endoplasmic reticulum membrane | 4 | 7 |
GO:0016020 | membrane | 2 | 7 |
GO:0031090 | organelle membrane | 3 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A4H978
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022406 | membrane docking | 2 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051640 | organelle localization | 2 | 1 |
GO:0051643 | endoplasmic reticulum localization | 3 | 1 |
GO:0061024 | membrane organization | 4 | 1 |
GO:0061817 | endoplasmic reticulum-plasma membrane tethering | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090158 | endoplasmic reticulum membrane organization | 5 | 1 |
GO:0140056 | organelle localization by membrane tethering | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 173 | 175 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.242 |
CLV_PCSK_PC1ET2_1 | 173 | 175 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.396 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.808 |
DEG_SPOP_SBC_1 | 201 | 205 | PF00917 | 0.714 |
DOC_MAPK_gen_1 | 128 | 135 | PF00069 | 0.594 |
DOC_MAPK_gen_1 | 37 | 47 | PF00069 | 0.571 |
DOC_MAPK_MEF2A_6 | 263 | 270 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 88 | 97 | PF00069 | 0.546 |
DOC_PP1_RVXF_1 | 241 | 248 | PF00149 | 0.635 |
DOC_PP4_FxxP_1 | 184 | 187 | PF00568 | 0.614 |
DOC_PP4_FxxP_1 | 54 | 57 | PF00568 | 0.546 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.802 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.478 |
DOC_USP7_UBL2_3 | 254 | 258 | PF12436 | 0.776 |
DOC_USP7_UBL2_3 | 40 | 44 | PF12436 | 0.542 |
DOC_WW_Pin1_4 | 143 | 148 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.720 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.795 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.671 |
LIG_14-3-3_CanoR_1 | 105 | 111 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 128 | 134 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 37 | 47 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 4 | 8 | PF00244 | 0.771 |
LIG_BRCT_BRCA1_1 | 243 | 247 | PF00533 | 0.636 |
LIG_EVH1_2 | 55 | 59 | PF00568 | 0.546 |
LIG_FHA_1 | 113 | 119 | PF00498 | 0.560 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.702 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.459 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.504 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.582 |
LIG_FHA_2 | 170 | 176 | PF00498 | 0.629 |
LIG_Integrin_RGD_1 | 157 | 159 | PF01839 | 0.497 |
LIG_LIR_Apic_2 | 183 | 187 | PF02991 | 0.684 |
LIG_LIR_Gen_1 | 104 | 113 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 149 | 156 | PF02991 | 0.613 |
LIG_LIR_Gen_1 | 188 | 197 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 104 | 110 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 149 | 154 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 188 | 192 | PF02991 | 0.630 |
LIG_MYND_1 | 143 | 147 | PF01753 | 0.698 |
LIG_SH2_PTP2 | 189 | 192 | PF00017 | 0.650 |
LIG_SH2_STAT3 | 312 | 315 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.613 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.650 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.546 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.678 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.616 |
LIG_SH3_3 | 50 | 56 | PF00018 | 0.543 |
LIG_SH3_3 | 87 | 93 | PF00018 | 0.524 |
LIG_SUMO_SIM_anti_2 | 188 | 194 | PF11976 | 0.562 |
LIG_SUMO_SIM_anti_2 | 279 | 284 | PF11976 | 0.512 |
LIG_SxIP_EBH_1 | 186 | 199 | PF03271 | 0.577 |
LIG_WRC_WIRS_1 | 181 | 186 | PF05994 | 0.685 |
LIG_WW_1 | 186 | 189 | PF00397 | 0.630 |
MOD_CDK_SPK_2 | 143 | 148 | PF00069 | 0.628 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.546 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.727 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.737 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.728 |
MOD_CK1_1 | 241 | 247 | PF00069 | 0.575 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.494 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.712 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.639 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.794 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.333 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.638 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.524 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.429 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.448 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.419 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.765 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.552 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.672 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.659 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.701 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.737 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.523 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.594 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.542 |
MOD_N-GLC_1 | 231 | 236 | PF02516 | 0.556 |
MOD_N-GLC_1 | 70 | 75 | PF02516 | 0.346 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.563 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.572 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.638 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.294 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.511 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.625 |
MOD_NEK2_2 | 180 | 185 | PF00069 | 0.685 |
MOD_PIKK_1 | 26 | 32 | PF00454 | 0.715 |
MOD_PIKK_1 | 311 | 317 | PF00454 | 0.573 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.626 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.590 |
MOD_PKA_2 | 3 | 9 | PF00069 | 0.773 |
MOD_Plk_2-3 | 137 | 143 | PF00069 | 0.611 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.630 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.626 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.442 |
MOD_ProDKin_1 | 143 | 149 | PF00069 | 0.627 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.719 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.688 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.796 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.480 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.672 |
MOD_SUMO_for_1 | 45 | 48 | PF00179 | 0.546 |
TRG_DiLeu_BaEn_1 | 48 | 53 | PF01217 | 0.546 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.650 |
TRG_NES_CRM1_1 | 123 | 137 | PF08389 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 119 | 123 | PF00026 | 0.442 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILZ1 | Leptomonas seymouri | 53% | 97% |
A0A3S5H717 | Leishmania donovani | 65% | 77% |
A4HXJ8 | Leishmania infantum | 65% | 77% |
E9AR93 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 81% |
Q4QE70 | Leishmania major | 65% | 100% |