GapMind for catabolism of small carbon sources

 

Alignments for a candidate for mmsA in Dyella japonica UNC79MFTsu3.2

Align Methylmalonate-semialdehyde dehydrogenase (EC 1.2.1.27) (characterized)
to candidate N515DRAFT_4224 N515DRAFT_4224 coniferyl-aldehyde dehydrogenase

Query= reanno::psRCH2:GFF2388
         (503 letters)



>FitnessBrowser__Dyella79:N515DRAFT_4224
          Length = 456

 Score =  110 bits (276), Expect = 8e-29
 Identities = 107/379 (28%), Positives = 158/379 (41%), Gaps = 15/379 (3%)

Query: 71  RARIFLKYQQLIRENMKELAAILTAEQGKTLADAEG--DVFRGLEVVEHAAGIGNLQLGE 128
           RAR       LI E+  E+A  +  + G   A      +VF  L  + HA   G   +  
Sbjct: 16  RARRLRALNDLIGEHRGEIADAIHQDFGGRPAQETDLLEVFPSLSAIRHALAHGRRWMKP 75

Query: 129 LAN---NVAAGVDTYTLLQPLGVCAGITPFNFPAMIPLWMFPMAIATGNTFVLKPSEQDP 185
             +    +          QPLGV   I P+N+P  +       A+A GN  ++K SE  P
Sbjct: 76  RRSWPGLLFMPARNEIRPQPLGVVGIIVPWNYPLFLAAGPMVDALAAGNRVMVKMSEYTP 135

Query: 186 MVTMRLCELALEAGVPPGVLNVVHGGPDVVNAICDHPDIKAVSFVGSTKVGTHVYNRASQ 245
             +    +LA     P  V  VV G  DV  A    P    + F GST VG HV   AS 
Sbjct: 136 QFSALFAQLAARYFKPEEVC-VVTGDADVAQAFSALP-FDHLLFTGSTAVGRHVMRAASA 193

Query: 246 AGKRVQCMMGAKNHAIVLPDAHKEQTLNNLAGAAFGAAGQRCMALSVVVLVGEAQAWIPD 305
               V   +G K+ AIV P A     +  +       AGQ C+A   V+L    +A + +
Sbjct: 194 NLTPVTLELGGKSPAIVGPGARFANAVERILVGKLFNAGQTCIAPDYVLL---PRAQVDE 250

Query: 306 LVAKAQTLKVNAGVEA--GTDVGPLVSCAALDRVSGLIERGVREGAKLELDGRNPSVSGY 363
            VA A+ +      +         ++S     R++ L +   R+GAKL L G        
Sbjct: 251 FVAAARDVAARLYPQPVRNEQYASIISERQYQRLAALRDDAARDGAKLTLLGDETDDIQR 310

Query: 364 ENGNFVGPTIFSGVTREMSVYQEEIFGPVLCVMAAATMDEAIELINANPNGNGTAIFTRS 423
                + P + +GV+  M+V QEEIFGP+L ++    +++AI  + A+P+     +F   
Sbjct: 311 RR---MTPALLTGVSESMAVMQEEIFGPLLPLVPYDDIEQAIAYVAAHPHPLALYLFEED 367

Query: 424 GAAARHFQEEIDVGQVGIN 442
           GA           G V IN
Sbjct: 368 GALVDRVLARTTAGGVTIN 386


Lambda     K      H
   0.318    0.134    0.394 

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: 506
Number of extensions: 20
Number of successful extensions: 4
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: 503
Length of database: 456
Length adjustment: 34
Effective length of query: 469
Effective length of database: 422
Effective search space:   197918
Effective search space used:   197918
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 (21.7 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Sep 17 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