GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Azospirillum brasilense Sp245

Align L-threonine dehydrogenase (EC 1.1.1.103) (characterized)
to candidate AZOBR_RS32240 AZOBR_RS32240 acetaldehyde dehydrogenase

Query= ecocyc::EG12293-MONOMER
         (383 letters)



>FitnessBrowser__azobra:AZOBR_RS32240
          Length = 886

 Score =  198 bits (504), Expect = 4e-55
 Identities = 135/372 (36%), Positives = 192/372 (51%), Gaps = 39/372 (10%)

Query: 30  GFTRTLIVTDNMLTKLGMAGDVQKALEERNIFSVIYDGTQPNPTTENVAAGLKLLKENNC 89
           G  R LIVTD  L + G   +  + L+   +    +     +PT   V  GL L      
Sbjct: 476 GKKRCLIVTDRFLFENGHVDETVRILKGLGLAVETFFEVAADPTLAVVRRGLALANAFQP 535

Query: 90  DSVISLGGGSPHDCAKGIALVAANGGDI--------------RDYEGVDRSAKPQLPMIA 135
           D +++LGGGSP D AK I  V     D+              R Y       K Q   +A
Sbjct: 536 DVILALGGGSPMDAAK-IMWVMYEAPDVAFEDLALRFMDIRKRIYTFPKLGVKAQF--VA 592

Query: 136 INTTAGTASEMTRFCIITDEARHIKMAIVDKHVTPLLSVNDSSLMIGMPKSLTAATGMDA 195
           + TT+GT SE+T F ++TDE   IK  I D  +TP +++ D++L++ MPK LTAA G+DA
Sbjct: 593 VPTTSGTGSEVTPFAVVTDERTGIKYPIADYELTPNMAIIDANLVMDMPKGLTAAGGIDA 652

Query: 196 LTHAIEAYVSIAATPITDACALKAVTMIAENLPLA-VEDGSNAKAREAMAYAQFLAGMAF 254
           +THA+EAYVS+ A   TD  AL+A+ ++ E+LP A    G + KARE +  A  LAG+AF
Sbjct: 653 VTHALEAYVSVLANEYTDGQALQALKLLKEHLPSAYANGGKDPKAREQVHSAATLAGIAF 712

Query: 255 NNASLGYVHAMAHQLGGFYNLPHGVCNAVLLPHVQVFNS---------------KVAAAR 299
            NA LG  H+MAH+LG  ++LPHGV NA+L+ +V  +N+                   AR
Sbjct: 713 ANAFLGVCHSMAHKLGAEFHLPHGVANALLIANVIRYNAADIPTKQTAFSQYDRPKGVAR 772

Query: 300 LRDCAAAMGVNVTGKNDAEGAEACINAIRELAKKVDIPAGLRDLNVKEEDFA----VLAT 355
             + A  +G+   G  D E  E  +  + EL + +DIPA ++   V E +F      +A 
Sbjct: 773 YAEIARHLGLG--GSRDHERVETLVAWVEELKRTLDIPASIQAAGVPEAEFLARLDAIAE 830

Query: 356 NALKDACGFTNP 367
            A  D C   NP
Sbjct: 831 AAFDDQCTGANP 842


Lambda     K      H
   0.318    0.131    0.373 

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: 713
Number of extensions: 26
Number of successful extensions: 4
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: 383
Length of database: 886
Length adjustment: 36
Effective length of query: 347
Effective length of database: 850
Effective search space:   294950
Effective search space used:   294950
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 (21.8 bits)
S2: 53 (25.0 bits)

This GapMind analysis is from Sep 17 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