GapMind for catabolism of small carbon sources

 

Alignments for a candidate for galactonolactonase in Chryseobacterium angstadtii KM

Align D-galactono-lactonase (EC 3.1.1.-) (characterized)
to candidate WP_048505944.1 ACM46_RS07115 lactonase family protein

Query= reanno::pseudo13_GW456_L13:PfGW456L13_3314
         (389 letters)



>NCBI__GCF_001045465.1:WP_048505944.1
          Length = 379

 Score =  204 bits (519), Expect = 3e-57
 Identities = 124/364 (34%), Positives = 202/364 (55%), Gaps = 15/364 (4%)

Query: 23  AEDYQLLVGSYTAGQS-QGIYRLAFDSRTGQIDASPLQVIKSA-NPSWLTLSKDQRHLFV 80
           +++  + VGS+   ++ +GIY    D+  G++  S +  +K   NPS+LTLS + +++F 
Sbjct: 25  SQNTYVFVGSFNRDKATEGIYVYQLDTIKGKL--SKVTSLKGILNPSFLTLSPNGQYIFA 82

Query: 81  VNENGPGQTDPVGRVSSFAIDPKTHALSLISQVQSLGNEPTHSSLSIDGSHLFVSNYSVA 140
             E+   +T   G VSSF  +PK   L+ I+  +S G  P + S+  +G  L  +NY   
Sbjct: 83  CTES---KTPNAGSVSSFKFNPKDETLTFINSQKSGGENPVYVSVHQNGKWLVNANYKE- 138

Query: 141 EDPGGTLAVLPVAADGKLKAVVQMSSHPASRVNPERQASAHVHSTIPSPDGRYVFANDLG 200
               G+ ++ P+  DG ++  VQ        VN +RQ  +HVH+ + SPD  ++F  DLG
Sbjct: 139 ----GSASIYPIDDDGTIQPAVQNFQFSEGSVNKDRQDRSHVHAAVFSPDSDHLFLTDLG 194

Query: 201 ADKVFAYRFDPKANPELPLTPATPAFVQLPPGSGPRHLLFSADGKHAWLTMEMSAQVAVF 260
           ADK+ +Y FD  ++   P   A   ++Q   GSGPRHL F  +GK+A+   E+S  V  +
Sbjct: 195 ADKIRSYTFD--SDKTEPAQAAKQPYIQSVLGSGPRHLTFHPNGKYAYCIEELSGTVNAY 252

Query: 261 DYHDGQLEQTQMVDLAAGQPVSDKAAAALHASADGKFLYVSNRGTANQLLVFAIDPATGH 320
            Y +  L+  Q V+    Q   +  ++ +H S DGKFLY +NRG  N + +F+I    G 
Sbjct: 253 QYENATLKSIQRVNTHTDQYKDNFESSDIHISPDGKFLYAANRGGENNIAIFSI-LEDGT 311

Query: 321 LSELQRRAVEGDHPREFSLDPSGKFLLIANQKSNQIVVVERDARTGLLGKTVQKLPMDAP 380
           L  +  ++  G H R F +D +GKFL++A+  S  +VV +RD +TGLL KT  K+ + + 
Sbjct: 312 LKNVGYQSTLGKHSRVFDIDETGKFLIVAHAGSGNLVVFKRDPQTGLLKKTGNKVKVKSA 371

Query: 381 SDLR 384
           S ++
Sbjct: 372 SSVK 375


Lambda     K      H
   0.316    0.132    0.382 

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: 410
Number of extensions: 24
Number of successful extensions: 8
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: 389
Length of database: 379
Length adjustment: 30
Effective length of query: 359
Effective length of database: 349
Effective search space:   125291
Effective search space used:   125291
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: 50 (23.9 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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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:

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:

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