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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4Q7V5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0007034 | vacuolar transport | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016192 | vesicle-mediated transport | 4 | 2 |
GO:0016197 | endosomal transport | 4 | 2 |
GO:0032509 | endosome transport via multivesicular body sorting pathway | 5 | 2 |
GO:0032511 | late endosome to vacuole transport via multivesicular body sorting pathway | 6 | 2 |
GO:0045324 | late endosome to vacuole transport | 5 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0071985 | multivesicular body sorting pathway | 5 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.561 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.487 |
DOC_CYCLIN_RxL_1 | 72 | 81 | PF00134 | 0.361 |
DOC_MAPK_gen_1 | 106 | 115 | PF00069 | 0.508 |
DOC_MAPK_MEF2A_6 | 106 | 115 | PF00069 | 0.487 |
DOC_MAPK_MEF2A_6 | 73 | 80 | PF00069 | 0.361 |
DOC_PP1_RVXF_1 | 73 | 80 | PF00149 | 0.297 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.436 |
DOC_WW_Pin1_4 | 60 | 65 | PF00397 | 0.392 |
LIG_14-3-3_CanoR_1 | 40 | 44 | PF00244 | 0.551 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.474 |
LIG_CaM_NSCaTE_8 | 82 | 89 | PF13499 | 0.252 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.408 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.390 |
LIG_GBD_Chelix_1 | 11 | 19 | PF00786 | 0.291 |
LIG_LIR_Gen_1 | 81 | 90 | PF02991 | 0.423 |
LIG_MYND_1 | 6 | 10 | PF01753 | 0.475 |
LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.444 |
LIG_SH2_STAT3 | 100 | 103 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.264 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.460 |
LIG_TRAF2_1 | 31 | 34 | PF00917 | 0.551 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.369 |
MOD_Cter_Amidation | 131 | 134 | PF01082 | 0.429 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.373 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.351 |
MOD_NEK2_1 | 85 | 90 | PF00069 | 0.320 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.155 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.551 |
MOD_Plk_4 | 111 | 117 | PF00069 | 0.354 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.361 |
MOD_Plk_4 | 17 | 23 | PF00069 | 0.410 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.416 |
MOD_ProDKin_1 | 60 | 66 | PF00069 | 0.392 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.361 |
TRG_ER_diArg_1 | 73 | 76 | PF00400 | 0.331 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM91 | Leptomonas seymouri | 70% | 98% |
A0A0S4IVS2 | Bodo saltans | 27% | 91% |
A0A1X0P3F9 | Trypanosomatidae | 45% | 100% |
A0A3Q8IDZ8 | Leishmania donovani | 94% | 100% |
A0A422N652 | Trypanosoma rangeli | 45% | 100% |
A4HHU9 | Leishmania braziliensis | 78% | 100% |
A4I4Z9 | Leishmania infantum | 94% | 100% |
E9B0C9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |