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: Q4QDZ3
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 7 |
GO:0016043 | cellular component organization | 3 | 7 |
GO:0022607 | cellular component assembly | 4 | 7 |
GO:0043933 | protein-containing complex organization | 4 | 7 |
GO:0051259 | protein complex oligomerization | 6 | 7 |
GO:0051260 | protein homooligomerization | 7 | 7 |
GO:0065003 | protein-containing complex assembly | 5 | 7 |
GO:0071840 | cellular component organization or biogenesis | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 242 | 244 | PF00675 | 0.501 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.315 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.457 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.501 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.395 |
DEG_APCC_DBOX_1 | 36 | 44 | PF00400 | 0.315 |
DOC_CYCLIN_RxL_1 | 276 | 283 | PF00134 | 0.408 |
DOC_MAPK_DCC_7 | 226 | 236 | PF00069 | 0.429 |
DOC_MAPK_gen_1 | 277 | 284 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 277 | 284 | PF00069 | 0.477 |
DOC_PP1_RVXF_1 | 240 | 247 | PF00149 | 0.520 |
DOC_PP2B_LxvP_1 | 282 | 285 | PF13499 | 0.400 |
DOC_PP2B_LxvP_1 | 86 | 89 | PF13499 | 0.315 |
DOC_PP4_FxxP_1 | 169 | 172 | PF00568 | 0.535 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.464 |
LIG_14-3-3_CanoR_1 | 208 | 215 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 279 | 285 | PF00244 | 0.399 |
LIG_14-3-3_CanoR_1 | 36 | 41 | PF00244 | 0.395 |
LIG_14-3-3_CanoR_1 | 85 | 89 | PF00244 | 0.345 |
LIG_APCC_ABBAyCdc20_2 | 242 | 248 | PF00400 | 0.525 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.460 |
LIG_CSL_BTD_1 | 135 | 138 | PF09270 | 0.378 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.682 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.500 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.331 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.395 |
LIG_LIR_Apic_2 | 167 | 172 | PF02991 | 0.510 |
LIG_LIR_Gen_1 | 94 | 102 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 101 | 107 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 94 | 98 | PF02991 | 0.354 |
LIG_SH2_NCK_1 | 105 | 109 | PF00017 | 0.395 |
LIG_SH2_SRC | 76 | 79 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.315 |
LIG_SH3_1 | 226 | 232 | PF00018 | 0.430 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.382 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.683 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.614 |
LIG_SUMO_SIM_par_1 | 259 | 264 | PF11976 | 0.513 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.395 |
LIG_WW_2 | 229 | 232 | PF00397 | 0.549 |
MOD_CK1_1 | 216 | 222 | PF00069 | 0.586 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.502 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.395 |
MOD_CK2_1 | 84 | 90 | PF00069 | 0.247 |
MOD_Cter_Amidation | 240 | 243 | PF01082 | 0.516 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.495 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.546 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.756 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.658 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.352 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.645 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.545 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.693 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.408 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.490 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.415 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.461 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.380 |
MOD_NEK2_1 | 246 | 251 | PF00069 | 0.447 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.315 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.461 |
MOD_NEK2_2 | 221 | 226 | PF00069 | 0.397 |
MOD_PIKK_1 | 139 | 145 | PF00454 | 0.440 |
MOD_PIKK_1 | 246 | 252 | PF00454 | 0.435 |
MOD_PKA_1 | 36 | 42 | PF00069 | 0.395 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.637 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.435 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.395 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.345 |
MOD_Plk_1 | 110 | 116 | PF00069 | 0.467 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.467 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.380 |
MOD_Plk_4 | 164 | 170 | PF00069 | 0.584 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.374 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.428 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.450 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.315 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.315 |
TRG_DiLeu_BaEn_1 | 94 | 99 | PF01217 | 0.350 |
TRG_DiLeu_BaEn_2 | 60 | 66 | PF01217 | 0.315 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.395 |
TRG_ER_diArg_1 | 125 | 127 | PF00400 | 0.526 |
TRG_ER_diArg_1 | 242 | 244 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 277 | 280 | PF00400 | 0.594 |
TRG_ER_diArg_1 | 36 | 38 | PF00400 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 41 | 45 | PF00026 | 0.345 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4Z1 | Leptomonas seymouri | 56% | 100% |
A0A3S5H729 | Leishmania donovani | 92% | 100% |
A4H9F7 | Leishmania braziliensis | 78% | 98% |
A4HXS4 | Leishmania infantum | 92% | 100% |
E9ARI6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |