GapMind for catabolism of small carbon sources

 

Alignments for a candidate for rocD in Methylovulum miyakonense HT12

Align Ornithine aminotransferase; OAT; EC 2.6.1.13; Ornithine--oxo-acid aminotransferase (uncharacterized)
to candidate WP_019866214.1 METMI_RS0110330 aspartate aminotransferase family protein

Query= curated2:C3P3K3
         (396 letters)



>NCBI__GCF_000384075.1:WP_019866214.1
          Length = 463

 Score =  228 bits (581), Expect = 3e-64
 Identities = 150/394 (38%), Positives = 212/394 (53%), Gaps = 51/394 (12%)

Query: 28  KAEGVWVEDPEGNRYMDLLSAYSAVNQGHRHPKIINAL-----IDQANRVTLTSRAFHSD 82
           +A G ++ D  G  Y+DLLS +     G  HP +I+AL     ++  N V L      S 
Sbjct: 43  RAVGQYLYDQNGTEYLDLLSGFGVFAIGRNHPTVISALQETLTLELPNLVQLDVSVL-SG 101

Query: 83  QLGPWYEKVAKLT--NKEMVLPMNTGAEAVETAIKTARRWAYDVKKVEANRAEIIVCEDN 140
            LG   +++ K T  N   +   N+G EAVE AIK AR   Y  K     R +I+ CE  
Sbjct: 102 LLG---QEIVKTTPENLNKIFFCNSGTEAVEAAIKFAR---YTTK-----REKIVFCEHG 150

Query: 141 FHGRTMGAVSMSSNEEYKRGFGPMLPGIIVIPYGDLEALKAAITP-NTAAFILEPIQGEA 199
           +HG TMG++S++    ++ GFGP+LPG   IP+ DL AL+AA++  + AAFI+EPIQG+ 
Sbjct: 151 YHGLTMGSLSLNGENIFREGFGPLLPGCSAIPFNDLGALEAALSQKDVAAFIVEPIQGK- 209

Query: 200 GINIPPAGFLKEALEVCKKENVLFVADEIQTGLGRTGKVFACDWDNVTPDMYILGKALGG 259
           G+N+P   +L E   +CK+   LFVADE+QTGLGRTGK +A D  NV+PDM  + KAL G
Sbjct: 210 GVNLPDDNYLPEVERLCKQYGTLFVADEVQTGLGRTGKFWAVDHWNVSPDMICMAKALSG 269

Query: 260 GVFPISCAAANRDILGVF-----EPGSHGSTFGGNPLACAVSIAALEVLEEEKLTERSLQ 314
           G  P+   A  + I+            HGSTF  N +A A  +A L VL EEKL +   +
Sbjct: 270 GFVPVGAVAITQKIMDTVYNRMDRAVVHGSTFSKNNMAMAAGLATLHVLAEEKLVDNCAK 329

Query: 315 LGEKLVGQLKEIDN--PMITEVRGKGLFIGIELNEP----ARPYCEQLKAA--GLLC--- 363
           +G  ++  L  +      + E RGKG+ I IE   P     +     L+AA  GL C   
Sbjct: 330 VGTDIINSLNAMSGKYEFLKEARGKGMMIAIEFKSPKSLTLKAAWAMLEAANKGLFCQMI 389

Query: 364 -----KETH---------ENVIRIAPPLVISEED 383
                KE H          NV+++ PPL ++++D
Sbjct: 390 TIPLFKEHHILTQVAGHGMNVVKLLPPLNLTQQD 423


Lambda     K      H
   0.317    0.136    0.402 

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: 413
Number of extensions: 20
Number of successful extensions: 7
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: 396
Length of database: 463
Length adjustment: 32
Effective length of query: 364
Effective length of database: 431
Effective search space:   156884
Effective search space used:   156884
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: 51 (24.3 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