Align trehalose-6-P hydrolase (TreA;BlTreA;BLi00797;BL03069) (EC 3.2.1.93) (characterized)
to candidate WP_010443333.1 G7G_RS0120445 DUF3459 domain-containing protein
Query= CAZy::AAU39732.1 (562 letters) >NCBI__GCF_000192475.1:WP_010443333.1 Length = 551 Score = 305 bits (782), Expect = 2e-87 Identities = 178/534 (33%), Positives = 279/534 (52%), Gaps = 56/534 (10%) Query: 8 WWKKAVVYQIYPKSFKDTTGNGVGDIRGIIEKLDYIKELACDVIWLTPIYQSPQNDNGYD 67 WW+ V+YQIYP+SF+D+ G+G+GD++GI ++L YI L D IW++P ++SP D GYD Sbjct: 19 WWRGGVIYQIYPRSFQDSNGDGIGDLKGITQRLGYIASLGVDAIWISPFFKSPMKDFGYD 78 Query: 68 ISDYYSIHEEYGTMADFEELLEEAHKRGIKVIMDLVVNHTSTEHRWFKEAASGKENLYRD 127 +SDY + +GTMADF+ELL++AH G+KV++DLV++HTS +H WFKE+ + +EN D Sbjct: 79 VSDYRDVDPMFGTMADFKELLDQAHAHGLKVMIDLVLSHTSDQHPWFKESRASRENPKSD 138 Query: 128 FYIWKDMKPNGAPPTNWESKFGGSAWEFHAESGQYYLHLYDVTQADLNWENEAVRKKVYE 187 +Y+W D KP+G PP NW S FGGSAW++ A QYYLH + +Q DLN+ + V+ + + Sbjct: 139 WYVWADPKPDGTPPNNWLSIFGGSAWQWDARRLQYYLHNFLTSQPDLNFHCKDVQDALLD 198 Query: 188 MMHFWFEKGIDGFRLDVINVISKDQRFPDDDEGDGRRFYTDGPRVHEFLNEMNRE--VFS 245 + FW + G+DGFRLD IN D + D+ G + +N N + ++S Sbjct: 199 VARFWLDLGVDGFRLDTINFYFHDAQLRDN---PGLPMDQRNASIAPMVNPYNHQDHLYS 255 Query: 246 KYDSMTVGEMSS-TTIAD------CIRYTNPESRELDMVFNFHHLKADYPNGEK--WALA 296 K + + + D C+ R L+++ +Y +G+K Sbjct: 256 KSQPENIAFLERLRALTDEYEGRACLGEVGDAQRGLEIM-------GEYTSGDKRMHMCY 308 Query: 297 DFDFLKLKKILSEW------QTEMNKGGGWNALFWCNHDQPRIVSRYG-DDGKYRKKSAK 349 F+FL+ + + + + Q E G W + NHD R SR+G DD R+ + Sbjct: 309 AFEFLEKRALTAAYAKQVFDQLEDKAGDAWPCWAFSNHDVQRHASRWGLDDAAVRQHAVL 368 Query: 350 MLATAIHMLQGTPYIYQGEELGM--TNPKFDDISLYRDVESLNMYRILKEAGKPEAEIIE 407 M+ L+G+ +YQGEELG+ + F+D+ +D + + PE Sbjct: 369 MMC-----LRGSACLYQGEELGLPEADVAFEDL---QDPYGIEFW--------PE----- 407 Query: 408 ILKAKSRDNSRTPVQWNG-EENAGFTAGTPWIPVPDNYKEINAEEALNDPDSIFYHYKKL 466 K RD RTP+ W +E +GF+AG PW+PV E + DP S+ +HY+ Sbjct: 408 ---FKGRDGCRTPMVWVAQDEQSGFSAGRPWLPVSATQAERAVDRLEQDPASMLHHYRHA 464 Query: 467 NELRKEFDIITTGDYQLILEDDQELYAYLRNGADEKLLVINNFYGKETEFQLPD 520 LR + +G Q + + + R E++ N + LP+ Sbjct: 465 IALRHAHSALMSGK-QTGMSQIGSVLTFTREDESEQVFCAFNLGDDPVDVTLPE 517 Lambda K H 0.317 0.137 0.424 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 893 Number of extensions: 45 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 562 Length of database: 551 Length adjustment: 36 Effective length of query: 526 Effective length of database: 515 Effective search space: 270890 Effective search space used: 270890 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.6 bits) S2: 53 (25.0 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory