Uncharacterized Protein, Uncharacterized
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. | yes | yes: 20 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4I6G2
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005509 | calcium ion binding | 5 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.327 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.460 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.460 |
CLV_PCSK_PC7_1 | 138 | 144 | PF00082 | 0.443 |
DOC_CKS1_1 | 209 | 214 | PF01111 | 0.569 |
DOC_MAPK_gen_1 | 104 | 113 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 106 | 115 | PF00069 | 0.399 |
DOC_PP2B_LxvP_1 | 168 | 171 | PF13499 | 0.524 |
DOC_PP4_FxxP_1 | 55 | 58 | PF00568 | 0.304 |
DOC_SPAK_OSR1_1 | 54 | 58 | PF12202 | 0.329 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.530 |
DOC_USP7_UBL2_3 | 92 | 96 | PF12436 | 0.329 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 208 | 213 | PF00397 | 0.583 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.630 |
LIG_AP2alpha_2 | 24 | 26 | PF02296 | 0.329 |
LIG_Clathr_ClatBox_1 | 115 | 119 | PF01394 | 0.382 |
LIG_deltaCOP1_diTrp_1 | 48 | 55 | PF00928 | 0.291 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.501 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.383 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.429 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.485 |
LIG_FHA_2 | 105 | 111 | PF00498 | 0.394 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.329 |
LIG_LIR_Apic_2 | 239 | 243 | PF02991 | 0.679 |
LIG_LIR_Apic_2 | 52 | 58 | PF02991 | 0.304 |
LIG_LIR_Gen_1 | 24 | 31 | PF02991 | 0.507 |
LIG_LIR_Nem_3 | 119 | 123 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 24 | 29 | PF02991 | 0.507 |
LIG_Pex14_1 | 49 | 53 | PF04695 | 0.421 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.544 |
LIG_SH2_CRK | 266 | 270 | PF00017 | 0.589 |
LIG_SH2_NCK_1 | 166 | 170 | PF00017 | 0.544 |
LIG_SH2_PTP2 | 194 | 197 | PF00017 | 0.518 |
LIG_SH2_PTP2 | 202 | 205 | PF00017 | 0.514 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 83 | 87 | PF00017 | 0.428 |
LIG_SH2_STAT3 | 210 | 213 | PF00017 | 0.583 |
LIG_SH2_STAT3 | 219 | 222 | PF00017 | 0.667 |
LIG_SH2_STAT3 | 253 | 256 | PF00017 | 0.620 |
LIG_SH2_STAT3 | 265 | 268 | PF00017 | 0.541 |
LIG_SH2_STAT3 | 274 | 277 | PF00017 | 0.520 |
LIG_SH2_STAT3 | 36 | 39 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 194 | 197 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 210 | 213 | PF00017 | 0.577 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.636 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 83 | 86 | PF00017 | 0.292 |
LIG_SH3_1 | 155 | 161 | PF00018 | 0.484 |
LIG_SH3_1 | 228 | 234 | PF00018 | 0.708 |
LIG_SH3_1 | 240 | 246 | PF00018 | 0.659 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.595 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.570 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.563 |
LIG_SH3_3 | 228 | 234 | PF00018 | 0.719 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.669 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.568 |
LIG_SUMO_SIM_par_1 | 114 | 119 | PF11976 | 0.549 |
LIG_TRAF2_1 | 124 | 127 | PF00917 | 0.446 |
LIG_TYR_ITIM | 200 | 205 | PF00017 | 0.513 |
LIG_TYR_ITIM | 264 | 269 | PF00017 | 0.523 |
LIG_WW_2 | 233 | 236 | PF00397 | 0.579 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.589 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.598 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.544 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.515 |
MOD_N-GLC_2 | 71 | 73 | PF02516 | 0.304 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.606 |
MOD_NEK2_2 | 49 | 54 | PF00069 | 0.362 |
MOD_PIKK_1 | 104 | 110 | PF00454 | 0.404 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.556 |
MOD_PIKK_1 | 268 | 274 | PF00454 | 0.527 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.329 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.335 |
MOD_Plk_1 | 4 | 10 | PF00069 | 0.329 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.627 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.535 |
MOD_ProDKin_1 | 208 | 214 | PF00069 | 0.583 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.565 |
MOD_SUMO_for_1 | 124 | 127 | PF00179 | 0.434 |
TRG_DiLeu_BaLyEn_6 | 111 | 116 | PF01217 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 193 | 198 | PF01217 | 0.528 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.502 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.352 |
TRG_Pf-PMV_PEXEL_1 | 114 | 119 | PF00026 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 12 | 16 | PF00026 | 0.372 |
TRG_Pf-PMV_PEXEL_1 | 143 | 147 | PF00026 | 0.445 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IFD2 | Leishmania donovani | 99% | 100% |
A0A3S7X485 | Leishmania donovani | 34% | 98% |
A0A3S7X4C0 | Leishmania donovani | 36% | 100% |
A4HJ46 | Leishmania braziliensis | 65% | 93% |
A4HJ57 | Leishmania braziliensis | 40% | 100% |
A4HJ58 | Leishmania braziliensis | 37% | 100% |
A4I6H2 | Leishmania infantum | 36% | 100% |
A4I6H3 | Leishmania infantum | 34% | 98% |
E9B1L9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9B1N0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
Q9BHE7 | Leishmania major | 35% | 100% |
Q9BHF8 | Leishmania major | 87% | 95% |