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: 1 |
NetGPI | no | yes: 0, no: 1 |
Related structures:
AlphaFold database: A4H8G2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.814 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 58 | 60 | PF00675 | 0.794 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.814 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.768 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.771 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.813 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.798 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.837 |
DOC_CYCLIN_RxL_1 | 54 | 64 | PF00134 | 0.793 |
DOC_MAPK_DCC_7 | 13 | 22 | PF00069 | 0.757 |
DOC_MAPK_gen_1 | 7 | 17 | PF00069 | 0.764 |
DOC_MAPK_MEF2A_6 | 13 | 22 | PF00069 | 0.757 |
DOC_PP2B_PxIxI_1 | 17 | 23 | PF00149 | 0.751 |
DOC_USP7_MATH_1 | 104 | 108 | PF00917 | 0.833 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.840 |
DOC_WW_Pin1_4 | 53 | 58 | PF00397 | 0.786 |
DOC_WW_Pin1_4 | 76 | 81 | PF00397 | 0.829 |
LIG_14-3-3_CanoR_1 | 28 | 35 | PF00244 | 0.756 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 7 | 17 | PF00244 | 0.764 |
LIG_BRCT_BRCA1_1 | 43 | 47 | PF00533 | 0.786 |
LIG_DLG_GKlike_1 | 43 | 51 | PF00625 | 0.793 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.841 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.754 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.834 |
LIG_Pex14_2 | 124 | 128 | PF04695 | 0.808 |
LIG_SH2_STAT3 | 26 | 29 | PF00017 | 0.746 |
LIG_SH3_3 | 12 | 18 | PF00018 | 0.754 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.829 |
MOD_CDK_SPxK_1 | 53 | 59 | PF00069 | 0.788 |
MOD_CDK_SPxxK_3 | 53 | 60 | PF00069 | 0.790 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.841 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.796 |
MOD_CK1_1 | 46 | 52 | PF00069 | 0.799 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.841 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.813 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.718 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.780 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.715 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.593 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.780 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.651 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.449 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.661 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.545 |
MOD_N-GLC_1 | 93 | 98 | PF02516 | 0.831 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.770 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.446 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.845 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.827 |
MOD_PIKK_1 | 97 | 103 | PF00454 | 0.844 |
MOD_PKA_2 | 27 | 33 | PF00069 | 0.753 |
MOD_Plk_1 | 93 | 99 | PF00069 | 0.833 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.751 |
MOD_Plk_4 | 22 | 28 | PF00069 | 0.545 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.797 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.841 |
MOD_ProDKin_1 | 53 | 59 | PF00069 | 0.788 |
MOD_ProDKin_1 | 76 | 82 | PF00069 | 0.830 |
TRG_DiLeu_BaLyEn_6 | 36 | 41 | PF01217 | 0.762 |
TRG_ER_diArg_1 | 35 | 37 | PF00400 | 0.765 |