GapMind for catabolism of small carbon sources

 

Alignments for a candidate for lctO in Rhizobium johnstonii 3841

Align Lactate 2-monooxygenase; EC 1.13.12.4; Lactate oxidase (uncharacterized)
to candidate WP_011651675.1 RL_RS10730 alpha-hydroxy acid oxidase

Query= curated2:P21795
         (394 letters)



>NCBI__GCF_000009265.1:WP_011651675.1
          Length = 395

 Score =  188 bits (478), Expect = 2e-52
 Identities = 127/373 (34%), Positives = 193/373 (51%), Gaps = 18/373 (4%)

Query: 29  DWEAHAQQALPPGVLSYVAGGSGDEHTQRANVEAFKHWGLMPRMLMAATERDLSVELWGK 88
           D+E  A++ LP  +  Y+AG +    + R N EAF+ +   PR+L   ++R     L+GK
Sbjct: 23  DFEIKARRHLPKPLFGYIAGATETNASLRHNAEAFQAYAFQPRVLRDVSKRSTETSLFGK 82

Query: 89  TWAAPMFFAPIGVIALCAQDGHGDAASAQASARTGVPYITSTLAVSSLEDIRKHAGDTPA 148
           T AAP   AP+G+ AL A    GD   AQ + ++G+P I S  ++  LE+I   A    A
Sbjct: 83  THAAPFGIAPMGISALMAY--RGDIVLAQGADQSGIPMIISGSSLIPLEEIA--AVSPQA 138

Query: 149 YFQLYYPEDRDLAESFIRRAEEAGYDGLVITLDTWIFGWRPRDLTIS-NFPFLRGLCLT- 206
           +FQ Y P + D  ++ I R   AG   L++T+DT     R  ++    + P   GL L  
Sbjct: 139 WFQAYLPGEPDRIDALIDRVGAAGLRTLLLTVDTATLPNRENNVRAGFSTPLRPGLRLAW 198

Query: 207 NYVTDP-----VFQKKFKAHSGVEAEG---LRDNPRLAADFWHGLFGHS--VTWEDIDWV 256
             ++ P      F +    H     E     R  P ++++     FG    + W  ++ +
Sbjct: 199 QGISHPRWTTGTFLRTIARHGIPHFENSYATRGAPIISSNVTRD-FGRRDHLNWNHLERI 257

Query: 257 RSITKMPVILKGIQHPDDARRAVDSGVDGIYCSNHGGRQANGGLPALDCLPEVVKASGDT 316
           R+     +++KGI HPDDA RAVD+G DG+  SNHGGRQ +G    L  LPE+    GD+
Sbjct: 258 RNRWSGKLVVKGIMHPDDAARAVDTGADGVIVSNHGGRQLDGTASPLQVLPEIASRVGDS 317

Query: 317 -PVLFDSGIRTGADVVKALAMGASAVGIGRPYAWGAALGGSKGIEHVARSLLAEADLIMA 375
             V+ D G R G D++KALA+GA  V +GRP+ + AA+ G  G+   A  L  E    MA
Sbjct: 318 VAVMVDGGFRRGTDIMKALALGARFVFVGRPFLYAAAVAGLPGVLKAADILKTELHSNMA 377

Query: 376 VDGYRNLKELTID 388
           + G   + +++ D
Sbjct: 378 LLGVTKVGDISAD 390


Lambda     K      H
   0.319    0.137    0.430 

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: 431
Number of extensions: 24
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 2
Length of query: 394
Length of database: 395
Length adjustment: 31
Effective length of query: 363
Effective length of database: 364
Effective search space:   132132
Effective search space used:   132132
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: 50 (23.9 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