GapMind for catabolism of small carbon sources

 

Alignments for a candidate for gcvT in Paraburkholderia bryophila 376MFSha3.1

Align Aminomethyltransferase; EC 2.1.2.10; Glycine cleavage system T protein (uncharacterized)
to candidate H281DRAFT_06542 H281DRAFT_06542 4-methylaminobutanoate oxidase (formaldehyde-forming)

Query= curated2:B8D1D7
         (357 letters)



>FitnessBrowser__Burk376:H281DRAFT_06542
          Length = 826

 Score =  153 bits (386), Expect = 2e-41
 Identities = 111/353 (31%), Positives = 179/353 (50%), Gaps = 29/353 (8%)

Query: 2   KKTPLFEIHKELGARLIEFHGWSM-----PVQYTSIIE--------------EHKAVRNQ 42
           +++PL+ + +E GA      GW       P +  + I+              EH+A R +
Sbjct: 431 RRSPLYALLREDGACFGSKMGWERANFFAPTRDEARIDYAFGQQNWLPLSGAEHRACRER 490

Query: 43  CGLFDVSHMGEILVEGPGALESLQKIVTNNVARLKKGQVLYTPMCKDDGGIIDDLLVYCL 102
             LFD++   + LV+G  A   LQ +V N+V  +  G  +YT M  + G    D  +  L
Sbjct: 491 VALFDMTSFSKFLVKGRDAQSVLQNLVANDVD-VPPGTTVYTGMLNERGNYESDFTLTRL 549

Query: 103 GQDKYLMVVNASNIEKDFNWVRDNSNQRTE---VVNESDNYALLALQGPNSKKILEKVSS 159
             D+YL+V   +   +DF+ + D +  R +   +V+ +  YA+LA+ GP S+++L+ VS 
Sbjct: 550 AADQYLLVTGTAQTTRDFDMI-DKAIPRDKHCVLVDVTSQYAVLAVMGPRSRELLQSVSK 608

Query: 160 VNL--DSLKFYNFTTGTLKGAEVLISRTGYTGELGYELYLSPDKAVEVWQALMEAGSDLG 217
            +   +S  F       +  A V  +R  Y GELG+ELY+  + AV V++ L EAG   G
Sbjct: 609 ADWRNESFAFGQSREVDIGYATVRATRLTYVGELGWELYVPVEFAVGVYEILHEAGKAFG 668

Query: 218 LIPAGLGARDTLRLEKGYCLYGNDIDENTHPLEAGLGWTVKFD-KASFIGKRALLKYKEE 276
           L+ AG  A D+LR+EKGY  +G ++  +T+P EA L +  K D    F G+ AL + + +
Sbjct: 669 LVNAGYYAIDSLRIEKGYRAWGRELTPDTNPFEAALAFACKLDTDIPFRGRDALAELRGK 728

Query: 277 GLSRKLVGFKLKGRG--IPRHGYPIKDNGDQIGVVTSGSMSPTLSEGIGMGYV 327
            L R++V     G    +   G  I  +G  +G V+S +   TL   + MGYV
Sbjct: 729 PLRRRMVVLTADGAADRMLWGGEAILRDGKPVGFVSSAAFGHTLGCPVAMGYV 781


Lambda     K      H
   0.317    0.138    0.404 

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: 686
Number of extensions: 30
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: 357
Length of database: 826
Length adjustment: 35
Effective length of query: 322
Effective length of database: 791
Effective search space:   254702
Effective search space used:   254702
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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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