GapMind for catabolism of small carbon sources

 

Alignments for a candidate for ARO8 in Escherichia coli BW25113

Align Aspartate aminotransferase; AspAT; Transaminase A; EC 2.6.1.1 (characterized)
to candidate 14737 b0600 putative aminotransferase (NCBI)

Query= SwissProt::Q9X0Y2
         (377 letters)



>FitnessBrowser__Keio:14737
          Length = 386

 Score =  175 bits (443), Expect = 2e-48
 Identities = 112/378 (29%), Positives = 191/378 (50%), Gaps = 17/378 (4%)

Query: 9   IPISKTMELDAKA---KALIKKGEDVINLTAGEPDFPTPEPVVEEAVRFLQKGEVKYTDP 65
           IP SK  +L        + + +    INL+ G PDF  P  + E     + +G  +Y   
Sbjct: 7   IPQSKLPQLGTTIFTQMSALAQQHQAINLSQGFPDFDGPRYLQERLAHHVAQGANQYAPM 66

Query: 66  RGIYELREGIAKRIGERYKKDISPDQ-VVVTNGAKQALFNAFMALLDPGDEVIVFSPVWV 124
            G+  LRE IA++    Y      D  + VT GA +AL+ A  AL+  GDEVI F P + 
Sbjct: 67  TGVQALREAIAQKTERLYGYQPDADSDITVTAGATEALYAAITALVRNGDEVICFDPSYD 126

Query: 125 SYIPQIILAGGTVNVVETFMSKNFQPSLEEVEGLLVGKTKAVLINSPNNPTGVVYRREFL 184
           SY P I L+GG V  +      +F+   +E   LL  +T+ V++N+P+NP+  V+++   
Sbjct: 127 SYAPAIALSGGIVKRM-ALQPPHFRVDWQEFAALLSERTRLVILNTPHNPSATVWQQADF 185

Query: 185 EGLVRLAKKRNFYIISDEVYDSLVYTDE-FTSILDVSEGFDRIVYINGFSKSHSMTGWRV 243
             L +       ++ISDEVY+ + ++ +   S+L   +  +R V ++ F K++ MTGW+V
Sbjct: 186 AALWQAIAGHEIFVISDEVYEHINFSQQGHASVLAHPQLRERAVAVSSFGKTYHMTGWKV 245

Query: 244 GYLISSEKVATAVSKIQSHTTSCINTVAQYAALKALEVDNSY---MVQTFKERKNFVVER 300
           GY ++   ++  + K+  + T  +NT AQ A    L  +  +   +   ++++++ +V  
Sbjct: 246 GYCVAPAPISAEIRKVHQYLTFSVNTPAQLALADMLRAEPEHYLALPDFYRQKRDILVNA 305

Query: 301 LKKMGVKFVEPEGAFYLFFKVRG----DDVKFCERLLEEKKVALVPGSAFLKPGF----V 352
           L +  ++ +  EG ++L          DDV+FC+ L +E  VA +P S F    F    +
Sbjct: 306 LNESRLEILPCEGTYFLLVDYSAVSTLDDVEFCQWLTQEHGVAAIPLSVFCADPFPHKLI 365

Query: 353 RLSFATSIERLTEALDRI 370
           RL FA     L  A +R+
Sbjct: 366 RLCFAKKESTLLAAAERL 383


Lambda     K      H
   0.319    0.137    0.384 

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: 295
Number of extensions: 17
Number of successful extensions: 5
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: 377
Length of database: 386
Length adjustment: 30
Effective length of query: 347
Effective length of database: 356
Effective search space:   123532
Effective search space used:   123532
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 (21.7 bits)
S2: 50 (23.9 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