Intracellular protein trafficking, transport Sec14, cytosolic factor
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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4ICS6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 53 | 57 | PF00656 | 0.421 |
CLV_MEL_PAP_1 | 98 | 104 | PF00089 | 0.449 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.330 |
CLV_PCSK_FUR_1 | 219 | 223 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.311 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.689 |
CLV_PCSK_PC1ET2_1 | 221 | 223 | PF00082 | 0.311 |
CLV_PCSK_PC1ET2_1 | 419 | 421 | PF00082 | 0.689 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 275 | 279 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 79 | 83 | PF00082 | 0.365 |
DEG_MDM2_SWIB_1 | 270 | 277 | PF02201 | 0.336 |
DEG_SCF_FBW7_1 | 388 | 395 | PF00400 | 0.661 |
DEG_SPOP_SBC_1 | 374 | 378 | PF00917 | 0.721 |
DEG_SPOP_SBC_1 | 392 | 396 | PF00917 | 0.562 |
DEG_SPOP_SBC_1 | 408 | 412 | PF00917 | 0.772 |
DOC_MAPK_gen_1 | 191 | 197 | PF00069 | 0.407 |
DOC_MAPK_gen_1 | 219 | 229 | PF00069 | 0.307 |
DOC_MAPK_gen_1 | 76 | 83 | PF00069 | 0.423 |
DOC_PP1_RVXF_1 | 132 | 139 | PF00149 | 0.421 |
DOC_PP1_RVXF_1 | 285 | 292 | PF00149 | 0.312 |
DOC_PP4_FxxP_1 | 291 | 294 | PF00568 | 0.366 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.611 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.372 |
DOC_USP7_UBL2_3 | 41 | 45 | PF12436 | 0.432 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 388 | 393 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.721 |
LIG_14-3-3_CanoR_1 | 105 | 110 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 191 | 196 | PF00244 | 0.361 |
LIG_APCC_ABBA_1 | 277 | 282 | PF00400 | 0.293 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.501 |
LIG_BRCT_BRCA1_1 | 386 | 390 | PF00533 | 0.643 |
LIG_CtBP_PxDLS_1 | 255 | 259 | PF00389 | 0.407 |
LIG_CtBP_PxDLS_1 | 345 | 349 | PF00389 | 0.354 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.407 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.660 |
LIG_FHA_1 | 90 | 96 | PF00498 | 0.478 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.479 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.473 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.399 |
LIG_FHA_2 | 347 | 353 | PF00498 | 0.452 |
LIG_FHA_2 | 5 | 11 | PF00498 | 0.510 |
LIG_LIR_Apic_2 | 341 | 346 | PF02991 | 0.570 |
LIG_LIR_Apic_2 | 377 | 383 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 108 | 117 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 126 | 136 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 108 | 112 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 126 | 132 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.340 |
LIG_PCNA_yPIPBox_3 | 116 | 129 | PF02747 | 0.436 |
LIG_PCNA_yPIPBox_3 | 288 | 302 | PF02747 | 0.423 |
LIG_Pex14_1 | 138 | 142 | PF04695 | 0.360 |
LIG_Pex14_2 | 270 | 274 | PF04695 | 0.293 |
LIG_SH2_CRK | 193 | 197 | PF00017 | 0.345 |
LIG_SH2_CRK | 343 | 347 | PF00017 | 0.576 |
LIG_SH2_NCK_1 | 343 | 347 | PF00017 | 0.561 |
LIG_SH2_NCK_1 | 87 | 91 | PF00017 | 0.484 |
LIG_SH2_SRC | 87 | 90 | PF00017 | 0.489 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.312 |
LIG_SH2_STAT3 | 149 | 152 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 162 | 165 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.247 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 70 | 73 | PF00017 | 0.293 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.294 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.750 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.469 |
LIG_TRAF2_1 | 398 | 401 | PF00917 | 0.684 |
LIG_UBA3_1 | 301 | 307 | PF00899 | 0.437 |
MOD_CDC14_SPxK_1 | 364 | 367 | PF00782 | 0.719 |
MOD_CDC14_SPxK_1 | 38 | 41 | PF00782 | 0.455 |
MOD_CDK_SPxK_1 | 35 | 41 | PF00069 | 0.423 |
MOD_CDK_SPxK_1 | 361 | 367 | PF00069 | 0.689 |
MOD_CK1_1 | 344 | 350 | PF00069 | 0.549 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.695 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.725 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.407 |
MOD_CK2_1 | 150 | 156 | PF00069 | 0.383 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.485 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.651 |
MOD_CK2_1 | 395 | 401 | PF00069 | 0.766 |
MOD_Cter_Amidation | 416 | 419 | PF01082 | 0.734 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.690 |
MOD_GlcNHglycan | 415 | 418 | PF01048 | 0.738 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.398 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.591 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.636 |
MOD_GSK3_1 | 403 | 410 | PF00069 | 0.661 |
MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.190 |
MOD_N-GLC_1 | 353 | 358 | PF02516 | 0.587 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.423 |
MOD_N-GLC_2 | 290 | 292 | PF02516 | 0.407 |
MOD_N-GLC_2 | 312 | 314 | PF02516 | 0.391 |
MOD_N-GLC_2 | 66 | 68 | PF02516 | 0.190 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.546 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.312 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.297 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.286 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.519 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.423 |
MOD_NEK2_2 | 365 | 370 | PF00069 | 0.696 |
MOD_PIKK_1 | 353 | 359 | PF00454 | 0.590 |
MOD_PKA_1 | 191 | 197 | PF00069 | 0.407 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.381 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.367 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.577 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.455 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.658 |
MOD_ProDKin_1 | 388 | 394 | PF00069 | 0.767 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.722 |
MOD_SUMO_rev_2 | 395 | 405 | PF00179 | 0.763 |
MOD_SUMO_rev_2 | 9 | 13 | PF00179 | 0.520 |
TRG_ENDOCYTIC_2 | 129 | 132 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 138 | 141 | PF00400 | 0.526 |
TRG_NLS_MonoCore_2 | 417 | 422 | PF00514 | 0.683 |
TRG_NLS_MonoExtN_4 | 418 | 423 | PF00514 | 0.681 |
TRG_NLS_MonoExtN_4 | 75 | 80 | PF00514 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 367 | 371 | PF00026 | 0.714 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PF64 | Leptomonas seymouri | 69% | 99% |
A0A0S4J1X8 | Bodo saltans | 46% | 100% |
A0A1X0P8J0 | Trypanosomatidae | 47% | 100% |
A0A3R7LCT9 | Trypanosoma rangeli | 48% | 100% |
A0A3S5H815 | Leishmania donovani | 99% | 100% |
E9ASH8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
P24859 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 25% | 100% |
V5BZX6 | Trypanosoma cruzi | 50% | 100% |