GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gly1 in Paraburkholderia bryophila 376MFSha3.1

Align L-threonine aldolase (EC 4.1.2.5) (characterized)
to candidate H281DRAFT_04448 H281DRAFT_04448 L-threonine aldolase

Query= reanno::pseudo3_N2E3:AO353_07670
         (346 letters)



>FitnessBrowser__Burk376:H281DRAFT_04448
          Length = 343

 Score =  462 bits (1190), Expect = e-135
 Identities = 219/341 (64%), Positives = 265/341 (77%), Gaps = 1/341 (0%)

Query: 6   QQFASDNYSGICPEAWAAMEQANQ-GHQRAYGDDEWTARASDDFRKLFETDCEVFFAFNG 64
           Q FASDNY+GICPEA  A+  AN  GH+ AYGDD WT +  D  R+LF+TDCEVFF FNG
Sbjct: 2   QHFASDNYAGICPEALHALIAANNSGHEPAYGDDSWTNQVCDRLRELFQTDCEVFFVFNG 61

Query: 65  TAANSLALSSLCQSYHSVICSETAHVETDECGAPEFFSNGSKLLIARTENGKLTPESIRE 124
           TAANSLAL+SLCQSYHSVIC E AH+ETDECG PEFFS GSKLL A    GKLTP++I  
Sbjct: 62  TAANSLALASLCQSYHSVICHELAHIETDECGGPEFFSGGSKLLTAPGIGGKLTPDAIEA 121

Query: 125 IALKRQDIHYPKPRVVTLTQATEVGSIYTPEEIRAISATCKELGLNLHMDGARFSNACAF 184
           +  +R DIHYPKP+VVTLTQ+TEVG++YT EE+RAI+A  K   L +HMDGARF+NA A 
Sbjct: 122 VVTRRADIHYPKPKVVTLTQSTEVGTVYTVEEVRAIAAIAKRRHLKVHMDGARFANAVAA 181

Query: 185 LNCSPADLTWKAGVDVLCFGGTKNGMAVGEAILFFNHKLAEDFDYRCKQAGQLASKMRFL 244
           L+  P+++TW+AGVDVLCFGGTKNG+ VGEA++FF+  LA DF YR KQAGQLASKMRF+
Sbjct: 182 LDVHPSEITWRAGVDVLCFGGTKNGLPVGEAVVFFDRALAADFAYRLKQAGQLASKMRFI 241

Query: 245 SAPWVGLLENDAWLKHARHANYCAQLLAELVSDIPGVELMFPVQANGVFLQLSESAVAAL 304
           SAPW+GLL+ND WL++ARHAN  AQLL   + +IPGV +MFP ++N VF QL   A  A+
Sbjct: 242 SAPWLGLLDNDVWLRNARHANAMAQLLQTRLQEIPGVSIMFPRESNAVFAQLPAQAAKAM 301

Query: 305 TAKSWRFYTFIGKGGARFMCSWDTEVERVRELAADIREVMA 345
            A  W+FY FIG GG R MC+WDT+ E V   A ++RE+ A
Sbjct: 302 RAHGWKFYEFIGAGGCRLMCAWDTQPETVERFATEVRELCA 342


Lambda     K      H
   0.320    0.132    0.408 

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: 427
Number of extensions: 11
Number of successful extensions: 2
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: 346
Length of database: 343
Length adjustment: 29
Effective length of query: 317
Effective length of database: 314
Effective search space:    99538
Effective search space used:    99538
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 (21.9 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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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