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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005739 | mitochondrion | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AK49
Term | Name | Level | Count |
---|---|---|---|
GO:0006996 | organelle organization | 4 | 2 |
GO:0007005 | mitochondrion organization | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.533 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.542 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.540 |
DEG_SPOP_SBC_1 | 27 | 31 | PF00917 | 0.562 |
DOC_PP4_MxPP_1 | 144 | 147 | PF00568 | 0.676 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.558 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.683 |
LIG_14-3-3_CanoR_1 | 26 | 35 | PF00244 | 0.577 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.519 |
LIG_Pex14_1 | 130 | 134 | PF04695 | 0.444 |
LIG_PTB_Apo_2 | 74 | 81 | PF02174 | 0.579 |
LIG_PTB_Phospho_1 | 74 | 80 | PF10480 | 0.604 |
LIG_SH2_SRC | 78 | 81 | PF00017 | 0.614 |
LIG_SH2_STAP1 | 114 | 118 | PF00017 | 0.399 |
LIG_SH2_STAT3 | 134 | 137 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.582 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.616 |
LIG_SH3_1 | 140 | 146 | PF00018 | 0.589 |
LIG_SH3_3 | 140 | 146 | PF00018 | 0.626 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.705 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.629 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.512 |
LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.622 |
MOD_CDK_SPxK_1 | 13 | 19 | PF00069 | 0.488 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.481 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.576 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.536 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.657 |
MOD_PIKK_1 | 106 | 112 | PF00454 | 0.368 |
MOD_PIKK_1 | 133 | 139 | PF00454 | 0.533 |
MOD_PIKK_1 | 85 | 91 | PF00454 | 0.566 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.611 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.548 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.686 |
TRG_ER_diArg_1 | 2 | 5 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 25 | 27 | PF00400 | 0.568 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NKW3 | Trypanosomatidae | 54% | 100% |
A0A3R7REF5 | Trypanosoma rangeli | 55% | 100% |
A0A3S5H5B8 | Leishmania donovani | 87% | 100% |
A0A3S5H5B9 | Leishmania donovani | 82% | 97% |
A4H401 | Leishmania braziliensis | 92% | 100% |
A4HS62 | Leishmania infantum | 86% | 100% |
A4HS63 | Leishmania infantum | 82% | 97% |
C9ZY60 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9AK50 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 97% |
Q9NED5 | Leishmania major | 95% | 100% |
Q9NED6 | Leishmania major | 91% | 100% |
V5BMV1 | Trypanosoma cruzi | 60% | 100% |