GapMind for catabolism of small carbon sources

 

Alignments for a candidate for davT in Sulfurivirga caldicuralii DSM 17737

Align 5-aminovalerate transaminase (EC 2.6.1.48) (characterized)
to candidate WP_074201116.1 BUQ81_RS04050 glutamate-1-semialdehyde 2,1-aminomutase

Query= BRENDA::Q9I6M4
         (426 letters)



>NCBI__GCF_900141795.1:WP_074201116.1
          Length = 432

 Score =  182 bits (463), Expect = 1e-50
 Identities = 121/335 (36%), Positives = 173/335 (51%), Gaps = 17/335 (5%)

Query: 25  PVVAERAENSTVWDVEGREYIDFAGGIAVLNTGHLHPKVIAAVQEQLGK-LSHTCFQVLA 83
           PV  +RA+ + VWDV+G+ YID+ G       GH HP+V+ AVQ+Q  K LS+       
Sbjct: 33  PVFIDRAKGAYVWDVDGKRYIDYVGSWGPAILGHAHPEVVEAVQKQAEKGLSYGA----P 88

Query: 84  YEPYIELAEEIAKRVPGDFPKKTLLVTSGSEAVENAVKIARAATGRAGVIAFTGAYHGRT 143
            E  +E+A+ I + +P        +V SG+EA   A+++AR ATGR  ++ F G YHG +
Sbjct: 89  TELEVEMADLICELIPS--VDMVRMVNSGTEATMTAIRLARGATGRDRIVKFEGGYHGHS 146

Query: 144 MMTLGLTGKVVPYSAGMGLMPGGIFRALAPCELHGVSEDDSIASIERIFKNDAQPQDIAA 203
              L   G     + G+   P G+ + LA   L     D     +  +F  D    +IA 
Sbjct: 147 DSLLVKAGSGA-LTHGVPSSP-GVPKCLAEQTLTLTYND--AEQVRNVF--DEVGDEIAC 200

Query: 204 IIIEPVQGEGGFYVNSKSFMQRLRALCDQHGILLIADEVQTGAGRTGTFFATEQLGIVPD 263
           II+EPV G          F++ LR +CD HG +LI DEV TG  R G   A  + GI PD
Sbjct: 201 IIVEPVAGNMNCIPPVPGFLETLRQVCDAHGAILIFDEVMTGF-RVGLTGAQGRYGITPD 259

Query: 264 LTTFAKSVGGGFPISGVAGKAEIMDAIAPGG---LGGTYAGSPIACAAALAVLKVFEEEK 320
           LTTF K +GGG P+  + GK EIM  +AP G     GT +G+P+A AA L  LK   +  
Sbjct: 260 LTTFGKVIGGGMPVGALGGKREIMSQLAPTGPVYQAGTLSGNPLAMAAGLTTLKRISQPG 319

Query: 321 LLERSQAVGERLKAGLREIQAKHKVIGDVRGLGSM 355
             E  +A  ++L  GL ++  +  +      +G M
Sbjct: 320 FFEDLEAKTQKLAMGLEQVAHEEGIALTTNQVGGM 354


Lambda     K      H
   0.319    0.137    0.393 

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: 449
Number of extensions: 29
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: 426
Length of database: 432
Length adjustment: 32
Effective length of query: 394
Effective length of database: 400
Effective search space:   157600
Effective search space used:   157600
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. 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