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: A4HIC0
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0008410 | CoA-transferase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016782 | transferase activity, transferring sulphur-containing groups | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.410 |
DOC_MAPK_DCC_7 | 201 | 210 | PF00069 | 0.570 |
DOC_MAPK_gen_1 | 161 | 171 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 75 | 83 | PF00069 | 0.610 |
DOC_PP1_RVXF_1 | 168 | 174 | PF00149 | 0.547 |
LIG_14-3-3_CanoR_1 | 135 | 144 | PF00244 | 0.547 |
LIG_CSL_BTD_1 | 98 | 101 | PF09270 | 0.610 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.539 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.610 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.610 |
LIG_GBD_Chelix_1 | 149 | 157 | PF00786 | 0.410 |
LIG_LIR_Apic_2 | 97 | 101 | PF02991 | 0.610 |
LIG_LIR_Gen_1 | 69 | 79 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 69 | 74 | PF02991 | 0.610 |
LIG_MAD2 | 135 | 143 | PF02301 | 0.610 |
LIG_SH2_STAT5 | 16 | 19 | PF00017 | 0.610 |
LIG_SH3_1 | 201 | 207 | PF00018 | 0.552 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.552 |
LIG_TRAF2_1 | 182 | 185 | PF00917 | 0.610 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.610 |
MOD_CK1_1 | 67 | 73 | PF00069 | 0.522 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.610 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.610 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.410 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.410 |
MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.322 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.400 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.610 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.497 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.610 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.472 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.610 |
MOD_NEK2_1 | 79 | 84 | PF00069 | 0.585 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.535 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.547 |
MOD_Plk_2-3 | 179 | 185 | PF00069 | 0.610 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.610 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.372 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.469 |
MOD_SUMO_rev_2 | 126 | 134 | PF00179 | 0.610 |
MOD_SUMO_rev_2 | 179 | 188 | PF00179 | 0.547 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
B0RVK3 | Xanthomonas campestris pv. campestris (strain B100) | 58% | 100% |
O34466 | Bacillus subtilis (strain 168) | 48% | 98% |
P0A101 | Pseudomonas putida (strain ATCC 47054 / DSM 6125 / CFBP 8728 / NCIMB 11950 / KT2440) | 48% | 100% |
P0A102 | Pseudomonas putida | 48% | 100% |
P0C7I8 | Xanthomonas campestris pv. campestris (strain ATCC 33913 / DSM 3586 / NCPPB 528 / LMG 568 / P 25) | 58% | 100% |
P23673 | Clostridium acetobutylicum (strain ATCC 824 / DSM 792 / JCM 1419 / LMG 5710 / VKM B-1787) | 42% | 96% |
P42316 | Bacillus subtilis (strain 168) | 56% | 99% |
P44874 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 43% | 96% |
P56007 | Helicobacter pylori (strain ATCC 700392 / 26695) | 53% | 100% |
P63651 | Mycobacterium bovis (strain ATCC BAA-935 / AF2122/97) | 53% | 98% |
P76459 | Escherichia coli (strain K12) | 45% | 99% |
P9WPW2 | Mycobacterium tuberculosis (strain CDC 1551 / Oshkosh) | 53% | 98% |
P9WPW3 | Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) | 53% | 98% |
Q59091 | Acinetobacter baylyi (strain ATCC 33305 / BD413 / ADP1) | 40% | 98% |
Q9ZLE4 | Helicobacter pylori (strain J99 / ATCC 700824) | 53% | 100% |