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: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: E9AK50
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 | 127 | 131 | PF00656 | 0.674 |
DOC_CKS1_1 | 32 | 37 | PF01111 | 0.670 |
DOC_PP4_MxPP_1 | 148 | 151 | PF00568 | 0.767 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.654 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.688 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.614 |
LIG_FHA_1 | 110 | 116 | PF00498 | 0.690 |
LIG_Pex14_1 | 134 | 138 | PF04695 | 0.541 |
LIG_PTB_Apo_2 | 78 | 85 | PF02174 | 0.661 |
LIG_PTB_Phospho_1 | 78 | 84 | PF10480 | 0.724 |
LIG_SH2_SRC | 82 | 85 | PF00017 | 0.734 |
LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.506 |
LIG_SH2_STAT3 | 138 | 141 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 138 | 141 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.622 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.736 |
LIG_SH3_1 | 144 | 150 | PF00018 | 0.700 |
LIG_SH3_2 | 21 | 26 | PF14604 | 0.623 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.752 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.646 |
LIG_SH3_3 | 36 | 42 | PF00018 | 0.705 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.673 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.623 |
LIG_TRAF2_1 | 104 | 107 | PF00917 | 0.740 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.640 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.610 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.696 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.673 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.630 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.656 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.647 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.676 |
MOD_PIKK_1 | 110 | 116 | PF00454 | 0.473 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.606 |
MOD_PIKK_1 | 89 | 95 | PF00454 | 0.713 |
MOD_PKA_2 | 8 | 14 | PF00069 | 0.690 |
MOD_Plk_4 | 70 | 76 | PF00069 | 0.569 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.682 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NKW3 | Trypanosomatidae | 48% | 100% |
A0A3S5H5B8 | Leishmania donovani | 95% | 100% |
A0A3S5H5B9 | Leishmania donovani | 97% | 100% |
A4H401 | Leishmania braziliensis | 86% | 100% |
A4HS62 | Leishmania infantum | 94% | 100% |
A4HS63 | Leishmania infantum | 97% | 100% |
C9ZY60 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9AK49 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
Q9NED5 | Leishmania major | 97% | 100% |
Q9NED6 | Leishmania major | 96% | 100% |
V5BMV1 | Trypanosoma cruzi | 52% | 100% |