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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 13 |
GO:0005815 | microtubule organizing center | 2 | 13 |
GO:0110165 | cellular anatomical entity | 1 | 13 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9ALG8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 113 | 117 | PF00656 | 0.540 |
CLV_C14_Caspase3-7 | 22 | 26 | PF00656 | 0.446 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.207 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.239 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.267 |
CLV_NRD_NRD_1 | 421 | 423 | PF00675 | 0.465 |
CLV_PCSK_FUR_1 | 279 | 283 | PF00082 | 0.264 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.262 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.241 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.258 |
CLV_PCSK_KEX2_1 | 336 | 338 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 421 | 423 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.200 |
CLV_PCSK_PC1ET2_1 | 225 | 227 | PF00082 | 0.251 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.258 |
CLV_PCSK_PC1ET2_1 | 336 | 338 | PF00082 | 0.254 |
CLV_PCSK_PC1ET2_1 | 400 | 402 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.313 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.406 |
DEG_SPOP_SBC_1 | 58 | 62 | PF00917 | 0.423 |
DOC_CYCLIN_yCln2_LP_2 | 293 | 299 | PF00134 | 0.522 |
DOC_CYCLIN_yCln2_LP_2 | 65 | 71 | PF00134 | 0.439 |
DOC_MAPK_MEF2A_6 | 291 | 299 | PF00069 | 0.360 |
DOC_PP2B_LxvP_1 | 293 | 296 | PF13499 | 0.491 |
DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.514 |
DOC_PP4_FxxP_1 | 94 | 97 | PF00568 | 0.448 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.420 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.416 |
DOC_USP7_UBL2_3 | 174 | 178 | PF12436 | 0.415 |
DOC_USP7_UBL2_3 | 221 | 225 | PF12436 | 0.431 |
DOC_USP7_UBL2_3 | 332 | 336 | PF12436 | 0.425 |
DOC_USP7_UBL2_3 | 386 | 390 | PF12436 | 0.454 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.435 |
LIG_14-3-3_CanoR_1 | 406 | 411 | PF00244 | 0.495 |
LIG_APCC_ABBA_1 | 370 | 375 | PF00400 | 0.442 |
LIG_BIR_III_2 | 116 | 120 | PF00653 | 0.565 |
LIG_BRCT_BRCA1_1 | 33 | 37 | PF00533 | 0.419 |
LIG_BRCT_BRCA1_1 | 55 | 59 | PF00533 | 0.429 |
LIG_BRCT_BRCA1_1 | 71 | 75 | PF00533 | 0.438 |
LIG_deltaCOP1_diTrp_1 | 403 | 410 | PF00928 | 0.487 |
LIG_EH_1 | 364 | 368 | PF12763 | 0.442 |
LIG_eIF4E_1 | 252 | 258 | PF01652 | 0.519 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.530 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.482 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.529 |
LIG_LIR_Apic_2 | 251 | 255 | PF02991 | 0.424 |
LIG_LIR_Apic_2 | 320 | 325 | PF02991 | 0.360 |
LIG_LIR_Gen_1 | 144 | 151 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 34 | 44 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 185 | 191 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 200 | 205 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 251 | 257 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 316 | 322 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.434 |
LIG_LYPXL_yS_3 | 254 | 257 | PF13949 | 0.507 |
LIG_MYND_1 | 46 | 50 | PF01753 | 0.382 |
LIG_Pex14_1 | 268 | 272 | PF04695 | 0.507 |
LIG_Pex14_2 | 143 | 147 | PF04695 | 0.481 |
LIG_Pex14_2 | 367 | 371 | PF04695 | 0.419 |
LIG_PTB_Apo_2 | 204 | 211 | PF02174 | 0.464 |
LIG_PTB_Apo_2 | 258 | 265 | PF02174 | 0.426 |
LIG_PTB_Phospho_1 | 204 | 210 | PF10480 | 0.507 |
LIG_PTB_Phospho_1 | 258 | 264 | PF10480 | 0.426 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.434 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.447 |
LIG_SH2_NCK_1 | 272 | 276 | PF00017 | 0.427 |
LIG_SH2_NCK_1 | 322 | 326 | PF00017 | 0.484 |
LIG_SH2_SRC | 163 | 166 | PF00017 | 0.510 |
LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 122 | 125 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 306 | 309 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 319 | 322 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.534 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.444 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.513 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.438 |
LIG_TRAF2_2 | 135 | 140 | PF00917 | 0.442 |
LIG_WW_2 | 46 | 49 | PF00397 | 0.393 |
MOD_CDC14_SPxK_1 | 245 | 248 | PF00782 | 0.382 |
MOD_CDK_SPxK_1 | 242 | 248 | PF00069 | 0.382 |
MOD_CDK_SPxxK_3 | 242 | 249 | PF00069 | 0.431 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.406 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.423 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.401 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.522 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.425 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.535 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.515 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.548 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.439 |
MOD_Cter_Amidation | 165 | 168 | PF01082 | 0.160 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.185 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.253 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.235 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.260 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.242 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.488 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.481 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.473 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.568 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.465 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.400 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.532 |
MOD_GSK3_1 | 351 | 358 | PF00069 | 0.481 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.444 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.430 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.434 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.424 |
MOD_N-GLC_1 | 125 | 130 | PF02516 | 0.307 |
MOD_N-GLC_1 | 355 | 360 | PF02516 | 0.307 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.413 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.454 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.535 |
MOD_NEK2_1 | 257 | 262 | PF00069 | 0.524 |
MOD_NEK2_1 | 351 | 356 | PF00069 | 0.456 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.525 |
MOD_NEK2_1 | 59 | 64 | PF00069 | 0.609 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.708 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.433 |
MOD_PIKK_1 | 11 | 17 | PF00454 | 0.433 |
MOD_PIKK_1 | 374 | 380 | PF00454 | 0.549 |
MOD_PKA_1 | 167 | 173 | PF00069 | 0.421 |
MOD_PKA_1 | 248 | 254 | PF00069 | 0.435 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.393 |
MOD_Plk_1 | 125 | 131 | PF00069 | 0.511 |
MOD_Plk_1 | 85 | 91 | PF00069 | 0.279 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.515 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.565 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.495 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.442 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.559 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.277 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.431 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.438 |
MOD_SUMO_for_1 | 335 | 338 | PF00179 | 0.442 |
MOD_SUMO_rev_2 | 101 | 109 | PF00179 | 0.420 |
MOD_SUMO_rev_2 | 110 | 117 | PF00179 | 0.436 |
MOD_SUMO_rev_2 | 140 | 148 | PF00179 | 0.378 |
MOD_SUMO_rev_2 | 162 | 169 | PF00179 | 0.432 |
MOD_SUMO_rev_2 | 215 | 222 | PF00179 | 0.491 |
TRG_DiLeu_BaEn_4 | 234 | 240 | PF01217 | 0.442 |
TRG_DiLeu_BaEn_4 | 393 | 399 | PF01217 | 0.360 |
TRG_DiLeu_BaLyEn_6 | 47 | 52 | PF01217 | 0.392 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 210 | 213 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 279 | 282 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 420 | 422 | PF00400 | 0.462 |
TRG_NLS_MonoCore_2 | 222 | 227 | PF00514 | 0.445 |
TRG_NLS_MonoExtC_3 | 222 | 227 | PF00514 | 0.398 |
TRG_NLS_MonoExtC_3 | 331 | 336 | PF00514 | 0.430 |
TRG_NLS_MonoExtN_4 | 221 | 227 | PF00514 | 0.428 |
TRG_NLS_MonoExtN_4 | 332 | 337 | PF00514 | 0.439 |
TRG_Pf-PMV_PEXEL_1 | 229 | 233 | PF00026 | 0.160 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6K0 | Leptomonas seymouri | 67% | 100% |
A0A0S4IPI4 | Bodo saltans | 38% | 100% |
A0A1X0P929 | Trypanosomatidae | 49% | 100% |
A0A3R7NAQ1 | Trypanosoma rangeli | 46% | 100% |
A0A3S7X2W5 | Leishmania donovani | 95% | 100% |
A4HGN9 | Leishmania braziliensis | 31% | 100% |
A4HHQ4 | Leishmania braziliensis | 80% | 99% |
A4I4W9 | Leishmania infantum | 95% | 100% |
C9ZKZ0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9AEB8 | Leishmania major | 94% | 100% |
V5DTV3 | Trypanosoma cruzi | 47% | 100% |