Aligments for a candidate for treF in Sphingomonas koreensis DSMZ 15582

GapMind for catabolism of small carbon sources

Aligments for a candidate for treF in Sphingomonas koreensis DSMZ 15582

Align alpha,alpha-trehalase (EC 3.2.1.28) (characterized)
to candidate Ga0059261_0579 Ga0059261_0579 Neutral trehalase

Query= BRENDA::P13482
         (565 letters)



>lcl|FitnessBrowser__Korea:Ga0059261_0579 Ga0059261_0579 Neutral
           trehalase
          Length = 495

 Score =  491 bits (1263), Expect = e-143
 Identities = 255/493 (51%), Positives = 319/493 (64%), Gaps = 5/493 (1%)

Query: 37  PQPPDILLGPLFNDVQNAKLFPDQKTFADAVPNSDPLMILADYRMQQNQSGFDLRHFVNV 96
           PQP D L G LF  VQ   LFPD KTFADAVP   P  I+ D++ Q       LR FV+ 
Sbjct: 4   PQPSD-LFGDLFTTVQECALFPDSKTFADAVPRRGPEAIMQDWKAQPPSGDAGLRAFVDA 62

Query: 97  NFTLPKEGEKYVPPEGQSLREHIDGLWPVLTRSTENTEKWDSLLPLPEPYVVPGGRFREV 156
           NF LP E +   P +G+ LREHI  LWPVLTR  E      SLL LP  +VVPGGRFRE+
Sbjct: 63  NFVLPTEADCDAP-DGRPLREHITQLWPVLTREPETPAPGSSLLALPRRHVVPGGRFREL 121

Query: 157 YYWDSYFTMLGLAESGHWDKVADMVANFAHEIDTYGHIPNGNRSYYLSRSQPPFFALMVE 216
           YYWDSYFTMLGL  S   D V DM+A F   +D YGHIPNG RSYYLSRS PP F LM  
Sbjct: 122 YYWDSYFTMLGLVRSDRQDLVEDMIAVFGSLLDGYGHIPNGTRSYYLSRSHPPVFYLMAA 181

Query: 217 LLAQHEGDAALKQYLPQMQKEYAYWMDGVENLQAGQQEKRVVKLQDGTLLNRYWDDRDTP 276
           L +Q     A  Q L  M+ E+ +WM G ++L  G + +RVV+L DG LLNRYWDDR  P
Sbjct: 182 L-SQDRSANARAQRLSWMRAEHEFWMAGEKDLAPGGEHRRVVRLADGALLNRYWDDRAAP 240

Query: 277 RPESWVEDIATAKSNPNRPATEIYRDLRSAAASGWDFSSRWMDNPQQLNTLRTTSIVPVD 336
           R ESW EDI  A+  P+R A E++RD+R+AA SGWDFSSRW+ + Q L T+RTT ++P+D
Sbjct: 241 RDESWREDIELAQRAPDRDAPELWRDIRAAAESGWDFSSRWLGDGQSLETIRTTRLLPID 300

Query: 337 LNSLMFKMEKILARASKAAGDNAMANQYETLANARQKGIEKYLWNDQQGWYADYDLKSHK 396
           LN+L+F +E+ +A  +KA GD+  A ++   A+AR++ I+ +LW+    +YADYDL   +
Sbjct: 301 LNALLFGLEQAIAEEAKALGDDTAATEFARRADARREAIDLHLWHPDAAFYADYDLDLGR 360

Query: 397 VRNQLTAAALFPLYVNAAAKDRANKMATATKTHLLQPGGLNTTSVKSGQQWDAPNGWAPL 456
              +LTAA  F L+   A+  RA   A A    LL+ GGL TT   +GQQWDAPNGWAPL
Sbjct: 361 ASGRLTAALGFALFTGVASAQRAPDAANAI-AGLLRAGGLLTTECVTGQQWDAPNGWAPL 419

Query: 457 QWVATEGLQNYGQKEVAMDISWHFLTNVQHTYDREKKLVEKYDVSTTGTGGGGGEYPLQD 516
            WV  EGL+ YGQ  +A  I+  +L  V   YD   +L+EKYD+      GGGGEY  + 
Sbjct: 420 HWVVIEGLRAYGQNALADTIAQRWLAMVASHYDATGQLLEKYDIEQC-RAGGGGEYGTEI 478

Query: 517 GFGWTNGVTLKML 529
           GFGWTNGVTL ++
Sbjct: 479 GFGWTNGVTLALM 491


Lambda     K      H
   0.315    0.132    0.409 

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: 874
Number of extensions: 42
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: 565
Length of database: 495
Length adjustment: 35
Effective length of query: 530
Effective length of database: 460
Effective search space:   243800
Effective search space used:   243800
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: 52 (24.6 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

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Steps (tab-delimited)
Rules (tab-delimited)
Protein sequences (fasta format)
Organisms (tab-delimited)
SQLite3 databases

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About GapMind

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:

ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
HMMer finds a hit (regardless of coverage or other bits).

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:

our ignorance of proteins' functions,
omissions in the gene models,
frame-shift errors in the genome sequence, or
the organism lacks the pathway.

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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.

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

GapMind for catabolism of small carbon sources