GapMind for catabolism of small carbon sources

 

Alignments for a candidate for astC in Brucella inopinata BO1

Align Succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_008511119.1 BIBO1_RS18855 aspartate aminotransferase family protein

Query= reanno::pseudo1_N1B4:Pf1N1B4_3440
         (406 letters)



>NCBI__GCF_000182725.1:WP_008511119.1
          Length = 442

 Score =  124 bits (311), Expect = 5e-33
 Identities = 118/416 (28%), Positives = 183/416 (43%), Gaps = 54/416 (12%)

Query: 32  AGSRVWDQSGRELIDFAGGIAVNVLGHAHPALVAALTEQANKLWHVSNV-FTNEPALRLA 90
           +G    D  G +++D   G+     GH    +  A+  Q + +         +  A   A
Sbjct: 34  SGMYYTDVDGNQVLDGTAGLWCCNAGHGRKRITEAVERQISTMDFAPTFQMGHNVAFDFA 93

Query: 91  HKLVDATFA------ERVFFCNSGAEANEAAFKLARRVAHDRF---GTEKYEIVAALNSF 141
            KL            +RVFF NSG+E+ + A K+A  +A+ R    GT    ++     +
Sbjct: 94  EKLAAIAPGGAEAKLDRVFFTNSGSESVDTALKIA--IAYQRAIGQGTRTM-VLGREKGY 150

Query: 142 HGRTLFTVNVGGQ---------------------SKYSDGFGPKITGITHVPYNDLAAL- 179
           HG     ++VGG                       K S   G    GI     +DL  L 
Sbjct: 151 HGVGFGGISVGGLVNNRRVFPQIPADHLRHTLDIEKNSFSKGLPANGIELA--DDLERLV 208

Query: 180 KAAVSDKTCAVVLEPIQGEGGVLPAELSYLQGARELCDAHNALLVFDEVQTGMGRSGKLF 239
           +   ++K  AV++EP+ G  GV+     YL+  R   D +  LL+FDEV TG GR G  F
Sbjct: 209 QLHGAEKIAAVIVEPMSGSAGVILPPKGYLERIRATADKYGILLIFDEVITGFGRLGTPF 268

Query: 240 AYQHYGVTPDILTSAKSL-GGGFPIAAMLTTEDLAKHLVVGT-------HGTTYGGNPLA 291
           A  ++GV PD++T+AK L  G  P+ A+     +   L+ G        HG TY G+P+A
Sbjct: 269 AVDYFGVVPDLVTTAKGLTNGAIPMGAVFAARKVYDGLMTGPENAIELFHGYTYSGHPVA 328

Query: 292 CAVAEAVIDVINTPEVLNGVNAKHDKFKTRLEQIGEKYGLFTEVRGLGLLLGCVLS---D 348
            A   A +++     +L       D ++  L  +     +  ++R LGL+    L+   D
Sbjct: 329 SAAGLATLEIYAEEGLLTRGAGLADYWQEALHSLKGAPNVI-DIRNLGLVGAVELASRKD 387

Query: 349 AWKGKAKDIFNAAEREGLMILQAGPDVIRFAPSLVVEDADIDAGL----DRFERAA 400
           A   +A DIF    ++GL+I   G DVI  +P L++E   ID  +    D  +RAA
Sbjct: 388 APGARAYDIFVECFKKGLLIRVTG-DVIALSPPLIIEKEQIDTIISVLGDAIKRAA 442


Lambda     K      H
   0.320    0.136    0.400 

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: 425
Number of extensions: 22
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: 406
Length of database: 442
Length adjustment: 32
Effective length of query: 374
Effective length of database: 410
Effective search space:   153340
Effective search space used:   153340
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 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