GapMind for catabolism of small carbon sources

 

Alignments for a candidate for davT in Methanococcus aeolicus Nankai-3

Align 5-aminovalerate transaminase (EC 2.6.1.48) (characterized)
to candidate WP_011973917.1 MAEO_RS06130 glutamate-1-semialdehyde 2,1-aminomutase

Query= BRENDA::Q9I6M4
         (426 letters)



>NCBI__GCF_000017185.1:WP_011973917.1
          Length = 432

 Score =  145 bits (365), Expect = 3e-39
 Identities = 116/339 (34%), Positives = 169/339 (49%), Gaps = 20/339 (5%)

Query: 25  PVVAERAENSTVWDVEGREYIDF--AGGIAVLNTGHLHPKVIAAVQEQLGKLSHTCFQVL 82
           P     A++  + DV+G +YID+  A G AVL  GH +  +  AV EQL    H      
Sbjct: 39  PFFVNNAKDYYLVDVDGNKYIDYCLAYGPAVL--GHANENIANAVIEQL---KHGTAYGC 93

Query: 83  AYEPYIELAEEIAKRVPGDFPKKTLLVTSGSEAVENAVKIARAATGRAGVIAFTGAYHGR 142
             E  I LA+EI KR+P    +    V SG+EA  +A+++AR  T R  +I F GAYHG 
Sbjct: 94  PTEKEITLAKEIIKRMP--CAEMVRFVNSGTEATMSAIRLARGITKRNKIIKFDGAYHGA 151

Query: 143 TMMTLGLTGKVVPYSAGMGLMPGGIFRALAPCELHGVSEDDSIASIERIFKNDAQPQDIA 202
               L  +G     + G    PG          L   ++ D+I  I    KN+    +IA
Sbjct: 152 HDYVLVKSGSGA-LTHGAPNSPGIPEDTTKHTILAPFNDKDAIVEI---IKNNKD--EIA 205

Query: 203 AIIIEPVQGEGGFYVNSKSFMQRLRALCDQHGILLIADEVQTGAGRTGTFFATEQLGIVP 262
            II+EPV G  G     + +++ LR + +++ I+LI DEV TG  R     A E  G+VP
Sbjct: 206 CIIVEPVMGNVGCIPPREDYLKFLREITEENNIILIFDEVITGF-RIAKGGAQEYYGVVP 264

Query: 263 DLTTFAKSVGGGFPISGVAGKAEIMDAIAPGGL---GGTYAGSPIACAAALAVLKVFEEE 319
           DL T  K +GGGFPI  + GK E+M+  +P G     GT+ G+PI+  A +  LK  ++ 
Sbjct: 265 DLATVGKIMGGGFPIGAIVGKKELMENFSPNGTIYQAGTFNGNPISMTAGIETLKNLDDN 324

Query: 320 KLLERSQAVGERLKAGLREIQAKHKVIGDVRGLGSMVAI 358
                S++  ++L   + E   KH +   V  + SM  I
Sbjct: 325 FYSTTSKS-AKKLSDFIGETAEKHNIPHKVYTVASMFQI 362


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: 398
Number of extensions: 23
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