GapMind for Amino acid biosynthesis

 

Alignments for a candidate for tyrB in Shewanella loihica PV-4

Align aspartate transaminase; EC 2.6.1.1 (characterized)
to candidate 5209443 Shew_1914 aminotransferase AlaT (RefSeq)

Query= CharProtDB::CH_004890
         (393 letters)



>FitnessBrowser__PV4:5209443
          Length = 404

 Score =  174 bits (440), Expect = 5e-48
 Identities = 114/386 (29%), Positives = 199/386 (51%), Gaps = 19/386 (4%)

Query: 21  KAKELKAAGHDVIGLGAGEP---DFNTPQHIIDAAVRSMNEGHTKYTPSGGLAELKNSIA 77
           +A+ L+  GH ++ L  G P    F  P+ I+   + ++      Y+ S GL   + +I 
Sbjct: 24  EARRLEDEGHRILKLNIGNPAPFGFEAPEEIVRDVILNLPSAQG-YSESKGLFSARKAIV 82

Query: 78  EKFKRDQNIEYKPSQIIVCTGAKHALYTLFQVILDEEDEVIIPTPYWVSYPEQVKLAGGK 137
           + ++           I +  G    +    Q +L+ +DEV++P+P +  +   V L+GGK
Sbjct: 83  QHYQSLGLFGVDIEDIYIGNGVSELIVMAMQGLLNSDDEVLVPSPDYPLWTAAVHLSGGK 142

Query: 138 PVYVEGLEENHFKISPEQLKNAITEKTKAIVINSPSNPTGVMYTEEELSALGEVCLEHDI 197
             +    EE+ +    + +K+ I+ +T+ IV+ +P+NPTG +Y+ E L  + E+C +HDI
Sbjct: 143 AQHYRCDEESDWFPDLDDIKSKISSRTRGIVLINPNNPTGAVYSRELLLEIIELCRQHDI 202

Query: 198 LIVSDEIYEKLTYGGKKHVSIAQLSDRLKEQTVIINGVSKSHSMTGWRIGY------AAG 251
           ++ +DEIY+K+ Y G  H+  A LSD +   TV  NG+SKS+   G+R+G+         
Sbjct: 203 ILFADEIYDKILYDGAVHIPAATLSDDI--LTVTFNGLSKSYRAAGFRVGWMMLSGNLKA 260

Query: 252 SEDIIKAMTNLASH--STSNPTSIAQYGAIAAYNGPSEPLEEMREAFEHRLNTIYAKLIE 309
           ++  I+ +  LAS    ++ P   A   A+  Y   +E L         + NT Y  L +
Sbjct: 261 AKSYIEGLDMLASMRLCSNVPNQHAIQTALGGYQSINE-LVAPEGRLTLQRNTCYELLNQ 319

Query: 310 IPGFSCVKPEGAFYLFPNAKEAAQSCGFKDVDEFVKALLEEEKVAIVPGSGFG--SPENV 367
           IPG SC KP+GA Y FP  K  A+    +D +  V  LL+E+K+ +V G+ F    P+++
Sbjct: 320 IPGVSCKKPKGALYAFP--KLDAKKFNLRDDERLVLDLLKEKKILLVQGTAFNWPEPDHL 377

Query: 368 RLSYATSLDLLEEAIERIKRFVEKHS 393
           R+ +    + L +A+     F+  +S
Sbjct: 378 RVVFLPHKEDLHKALVEFGDFLTSYS 403


Lambda     K      H
   0.313    0.131    0.370 

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: 398
Number of extensions: 19
Number of successful extensions: 3
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: 393
Length of database: 404
Length adjustment: 31
Effective length of query: 362
Effective length of database: 373
Effective search space:   135026
Effective search space used:   135026
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.2 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 42 (21.9 bits)
S2: 50 (23.9 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