GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gly1 in Desulfovibrio vulgaris Hildenborough

Align L-threonine aldolase (EC 4.1.2.5) (characterized)
to candidate 207344 DVU1878 threonine aldolase, low-specificity

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



>MicrobesOnline__882:207344
          Length = 340

 Score =  285 bits (728), Expect = 2e-81
 Identities = 152/339 (44%), Positives = 220/339 (64%), Gaps = 3/339 (0%)

Query: 6   QQFASDNYSGICPEAWAAMEQANQGHQRAYGDDEWTARASDDFRKLFETDCEVFFAFNGT 65
           + FASDN +G+ P   AAM  AN+GH +AYG D WT+ A+D FR  F  D +++F F GT
Sbjct: 3   KSFASDNTAGVHPRILAAMASANEGHAKAYGMDPWTSEAADVFRGHFGDDIDLYFVFLGT 62

Query: 66  AANSLALSSLCQSYHSVICSETAHVETDECGAPEFFSNGSKLLIARTENGKLTPESIREI 125
           AAN L L S+ + +HSV+C++ AH+  DECGAPE  + GSKL +  + +G++    I  +
Sbjct: 63  AANVLGLKSVTRPWHSVVCADVAHINVDECGAPESVT-GSKLQVIPSHDGRIRVMDIVPL 121

Query: 126 ALKRQDIHYPKPRVVTLTQATEVGSIYTPEEIRAISATCKELGLNLHMDGARFSNACAFL 185
                + H+ +PRV+++TQ TE+G++Y+P +IRA++      G+ LHMDGAR  NA A L
Sbjct: 122 MHSLGNFHHSQPRVISITQTTELGTVYSPAQIRALADFAHANGMLLHMDGARLCNAAAAL 181

Query: 186 NCSPADLTWKAGVDVLCFGGTKNGMAVGEAILFFNHKLAEDFDYRCKQAGQLASKMRFLS 245
           +   A LT   GVDVL FGGTKNGM  GEA++FFN +LA +F +  KQ  QL SKMRF++
Sbjct: 182 DTGLAALTRDTGVDVLSFGGTKNGMMFGEAVIFFNRELASEFKFIRKQGMQLVSKMRFIA 241

Query: 246 APWVGLLENDAWLKHARHANYCAQLLAELVSDIPGVELMFPVQANGVFLQLSESAVAALT 305
           A ++ LL +  WL++AR+AN  A+L+AE +  +P V +  PV+AN VF +LS   +AAL 
Sbjct: 242 AQFIELLRDGLWLENARNANSMARLMAESLRGLPHVTITRPVEANAVFARLSPEHIAAL- 300

Query: 306 AKSWRFYTFIG-KGGARFMCSWDTEVERVRELAADIREV 343
            K + FY +       R+M S+D+  E+V E    I+ +
Sbjct: 301 QKDFYFYEWDPVLHEVRWMTSFDSTEEQVMEFVHAIKRL 339


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: 289
Number of extensions: 7
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: 340
Length adjustment: 29
Effective length of query: 317
Effective length of database: 311
Effective search space:    98587
Effective search space used:    98587
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