GapMind for catabolism of small carbon sources

 

Alignments for a candidate for astC in Desulfobacter vibrioformis DSM 8776

Align Succinylornithine transaminase (EC 2.6.1.81) (characterized)
to candidate WP_035242472.1 Q366_RS19250 aspartate aminotransferase family protein

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



>NCBI__GCF_000745975.1:WP_035242472.1
          Length = 398

 Score =  318 bits (816), Expect = 1e-91
 Identities = 169/363 (46%), Positives = 228/363 (62%), Gaps = 2/363 (0%)

Query: 29  VRGAGSRVWDQSGRELIDFAGGIAVNVLGHAHPALVAALTEQANKLWHVSNVFTNEPALR 88
           V+G G++++D  G    DF  GIAV  LGH HP + AA++ QA  L HVSN+F   P   
Sbjct: 22  VKGRGTQLYDDQGNVYTDFLAGIAVCNLGHCHPDITAAISAQAGTLVHVSNLFYTRPQAE 81

Query: 89  LAHKLVDATFAERVFFCNSGAEANEAAFKLARRVAHDRFGTEKYEIVAALNSFHGRTLFT 148
           LA  L + +FA+RVFF NSGAEANEAA KLARR    +    +++IV    SFHGRT+ T
Sbjct: 82  LAKVLTEKSFADRVFFANSGAEANEAAIKLARRFFQAKGEAGRFKIVTMQQSFHGRTMAT 141

Query: 149 VNVGGQSKYSDGFGPKITGITHVPYNDLAALKAAVSDKTCAVVLEPIQGEGGVLPAELSY 208
           ++  GQ K   GF P + G  HVP+ND+ ALKA +    CAV++EP+QGEGGV+PA+  Y
Sbjct: 142 LSATGQDKIKKGFFPLLDGFIHVPFNDIEALKAVMDGTVCAVMMEPVQGEGGVIPADPEY 201

Query: 209 LQGARELCDAHNALLVFDEVQTGMGRSGKLFAYQHYGVTPDILTSAKSLGGGFPIAAMLT 268
           ++  R+LC     LL+FDE+QTGMGR G LFA++ Y V PDI+T AK+L  G PI AML 
Sbjct: 202 IKAVRQLCTDTGTLLIFDEIQTGMGRCGTLFAHESYDVVPDIMTLAKALANGVPIGAMLA 261

Query: 269 TEDLAKHLVVGTHGTTYGGNPLACAVAEAVIDVINTPEVLNGVNAKHDKFKTRLEQIGEK 328
           +E+ A    VG+HG+T+GG PLA A A  V+ +I+    L  V  K   F  +L  + EK
Sbjct: 262 SEEAALGFEVGSHGSTFGGTPLATAAALEVVRLISEQGFLASVREKSAYFLAQLNGLKEK 321

Query: 329 YGLFTEVRGLGLLLGCVLSDAWKGK-AKDIFNAAEREGLMILQAGPDVIRFAPSLVVEDA 387
           +    +VRG GLL+G  L D  KGK A D  +   ++G +I      V+RFAP L++   
Sbjct: 322 HKKVVDVRGKGLLIGMEL-DISKGKTATDYVSECFKKGFIINAIQDKVLRFAPPLIIGTV 380

Query: 388 DID 390
           +I+
Sbjct: 381 EIN 383


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: 360
Number of extensions: 11
Number of successful extensions: 1
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: 406
Length of database: 398
Length adjustment: 31
Effective length of query: 375
Effective length of database: 367
Effective search space:   137625
Effective search space used:   137625
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