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: 17 |
NetGPI | no | yes: 0, no: 17 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 18 |
GO:0005815 | microtubule organizing center | 2 | 18 |
GO:0110165 | cellular anatomical entity | 1 | 18 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7X2W5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 30 | 34 | PF00656 | 0.554 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 248 | 250 | PF00675 | 0.256 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.491 |
CLV_PCSK_FUR_1 | 195 | 199 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.270 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.307 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.290 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.303 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.271 |
CLV_PCSK_PC1ET2_1 | 248 | 250 | PF00082 | 0.281 |
CLV_PCSK_PC1ET2_1 | 252 | 254 | PF00082 | 0.300 |
CLV_PCSK_PC1ET2_1 | 316 | 318 | PF00082 | 0.381 |
CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.208 |
CLV_PCSK_SKI1_1 | 249 | 253 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.158 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.339 |
DOC_CYCLIN_yCln2_LP_2 | 209 | 215 | PF00134 | 0.537 |
DOC_PP2B_LxvP_1 | 209 | 212 | PF13499 | 0.508 |
DOC_PP4_FxxP_1 | 11 | 14 | PF00568 | 0.463 |
DOC_PP4_FxxP_1 | 213 | 216 | PF00568 | 0.465 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 216 | 220 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.540 |
DOC_USP7_UBL2_3 | 138 | 142 | PF12436 | 0.442 |
DOC_USP7_UBL2_3 | 248 | 252 | PF12436 | 0.441 |
DOC_USP7_UBL2_3 | 302 | 306 | PF12436 | 0.479 |
DOC_USP7_UBL2_3 | 91 | 95 | PF12436 | 0.422 |
LIG_14-3-3_CanoR_1 | 322 | 327 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 63 | 68 | PF00244 | 0.417 |
LIG_APCC_ABBA_1 | 286 | 291 | PF00400 | 0.449 |
LIG_BIR_III_2 | 33 | 37 | PF00653 | 0.578 |
LIG_deltaCOP1_diTrp_1 | 319 | 326 | PF00928 | 0.513 |
LIG_EH_1 | 280 | 284 | PF12763 | 0.449 |
LIG_eIF4E_1 | 168 | 174 | PF01652 | 0.534 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.499 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.538 |
LIG_LIR_Apic_2 | 167 | 171 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 61 | 68 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 102 | 108 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 117 | 122 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 232 | 238 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 5 | 10 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 61 | 67 | PF02991 | 0.425 |
LIG_LYPXL_yS_3 | 170 | 173 | PF13949 | 0.523 |
LIG_Pex14_1 | 184 | 188 | PF04695 | 0.523 |
LIG_Pex14_2 | 283 | 287 | PF04695 | 0.434 |
LIG_Pex14_2 | 60 | 64 | PF04695 | 0.473 |
LIG_PTB_Apo_2 | 121 | 128 | PF02174 | 0.481 |
LIG_PTB_Apo_2 | 174 | 181 | PF02174 | 0.442 |
LIG_PTB_Phospho_1 | 121 | 127 | PF10480 | 0.523 |
LIG_PTB_Phospho_1 | 174 | 180 | PF10480 | 0.442 |
LIG_SH2_CRK | 168 | 172 | PF00017 | 0.451 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.466 |
LIG_SH2_NCK_1 | 188 | 192 | PF00017 | 0.436 |
LIG_SH2_NCK_1 | 238 | 242 | PF00017 | 0.501 |
LIG_SH2_SRC | 80 | 83 | PF00017 | 0.495 |
LIG_SH2_STAP1 | 180 | 184 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 222 | 225 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.358 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.450 |
LIG_TRAF2_1 | 147 | 150 | PF00917 | 0.437 |
LIG_TRAF2_2 | 52 | 57 | PF00917 | 0.449 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.433 |
MOD_CK1_1 | 330 | 336 | PF00069 | 0.537 |
MOD_CK2_1 | 104 | 110 | PF00069 | 0.521 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.462 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.534 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.265 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.267 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.263 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.229 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.488 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.458 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.463 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.452 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.582 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.372 |
MOD_N-GLC_1 | 271 | 276 | PF02516 | 0.323 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.323 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.556 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.540 |
MOD_NEK2_1 | 267 | 272 | PF00069 | 0.433 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.545 |
MOD_PIKK_1 | 290 | 296 | PF00454 | 0.565 |
MOD_PKA_1 | 141 | 147 | PF00069 | 0.483 |
MOD_PKA_1 | 164 | 170 | PF00069 | 0.461 |
MOD_PKA_1 | 84 | 90 | PF00069 | 0.444 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.525 |
MOD_PKA_2 | 84 | 90 | PF00069 | 0.433 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.285 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.523 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.515 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.294 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.548 |
MOD_Plk_4 | 257 | 263 | PF00069 | 0.511 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.466 |
MOD_SUMO_for_1 | 251 | 254 | PF00179 | 0.449 |
MOD_SUMO_rev_2 | 132 | 139 | PF00179 | 0.480 |
MOD_SUMO_rev_2 | 18 | 26 | PF00179 | 0.436 |
MOD_SUMO_rev_2 | 27 | 34 | PF00179 | 0.452 |
MOD_SUMO_rev_2 | 79 | 86 | PF00179 | 0.401 |
TRG_DiLeu_BaEn_4 | 150 | 156 | PF01217 | 0.449 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.500 |
TRG_ENDOCYTIC_2 | 127 | 130 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.499 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.474 |
TRG_ER_diArg_1 | 195 | 198 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 336 | 338 | PF00400 | 0.496 |
TRG_NLS_MonoCore_2 | 139 | 144 | PF00514 | 0.461 |
TRG_NLS_MonoExtC_3 | 247 | 252 | PF00514 | 0.446 |
TRG_NLS_MonoExtN_4 | 138 | 145 | PF00514 | 0.445 |
TRG_NLS_MonoExtN_4 | 248 | 253 | PF00514 | 0.455 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6K0 | Leptomonas seymouri | 67% | 98% |
A0A0S4IPI4 | Bodo saltans | 37% | 100% |
A0A1X0P929 | Trypanosomatidae | 50% | 97% |
A0A3Q8IGT8 | Leishmania donovani | 30% | 100% |
A0A3R7NAQ1 | Trypanosoma rangeli | 47% | 99% |
A4HGN9 | Leishmania braziliensis | 30% | 100% |
A4HHQ4 | Leishmania braziliensis | 81% | 99% |
A4I3R2 | Leishmania infantum | 30% | 100% |
A4I4W9 | Leishmania infantum | 100% | 100% |
C9ZKZ0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 85% |
D0A995 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AEB8 | Leishmania major | 96% | 100% |
E9ALG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9B005 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
Q4Q880 | Leishmania major | 30% | 100% |
V5DTV3 | Trypanosoma cruzi | 48% | 99% |