GapMind for Amino acid biosynthesis

 

Alignments for a candidate for dapC in Synechococcus elongatus PCC 7942

Align phosphoserine transaminase (EC 2.6.1.52) (characterized)
to candidate Synpcc7942_0191 Synpcc7942_0191 Serine--glyoxylate transaminase

Query= BRENDA::P74281
         (384 letters)



>FitnessBrowser__SynE:Synpcc7942_0191
          Length = 382

 Score =  514 bits (1324), Expect = e-150
 Identities = 260/383 (67%), Positives = 308/383 (80%), Gaps = 1/383 (0%)

Query: 1   MDNKQMLMIPGPTPVPEKVLLAMAKHPIGHRSGDFSKIIAELTANLKWLHQTENDVLMLT 60
           M++K MLMIPGPTPVPE+VLLAMAKHPIGHRS DFS+++A+ TA LKWLHQT  +VL+L 
Sbjct: 1   MEDKLMLMIPGPTPVPEQVLLAMAKHPIGHRSADFSRLVADTTAGLKWLHQTTGNVLVLC 60

Query: 61  TSGTGAMEASIINFLSPGDRVLVGNNGKFGDRWVKVAKTFGLAVEEIKAEWGKALDPNDF 120
           +SGTGAMEA IINFLS GDRVL   NGKFG+RWVK+A+ FGL V+ ++A WGK LDP   
Sbjct: 61  SSGTGAMEAGIINFLSAGDRVLCCENGKFGERWVKLAQAFGLDVDLVQAPWGKPLDPEAI 120

Query: 121 KTLLEADSDKTIKALIITHSETSTGVLNDLAAINAAAKAHGGALMIVDAVTSLGATPVAI 180
           +  LEAD+DK IKA+I+THSETSTGV+NDL  I+   +AHG AL IVDAVTSLGA  V I
Sbjct: 121 RAKLEADTDKQIKAVILTHSETSTGVINDLETISGYIRAHG-ALSIVDAVTSLGAANVPI 179

Query: 181 DDLGLDVVASGSQKGYMIPPGLGFVSVSAKAWQAYETATIPRFYLDLKKYKKSTDEDSSP 240
           D  GLDVVASGSQKGYMIPPGLGFV+VS +AW+AYETAT+P+FYLDL KY+K+  +DS+P
Sbjct: 180 DAWGLDVVASGSQKGYMIPPGLGFVAVSDRAWKAYETATLPKFYLDLGKYRKAAQKDSNP 239

Query: 241 FTPPINLMYGLQASLQMMKAEGLDAIFTRHQRHTNATRGAMKALNLPLFAPDNAASNAIT 300
           FTPP+NL Y L A+L++M+ EGL+ IF RH + T ATR A+KALNLPL+A D   S AIT
Sbjct: 240 FTPPVNLYYALDAALKIMQREGLENIFARHAKLTRATRAAIKALNLPLYAADEVGSPAIT 299

Query: 301 AVAPLGVEAEKIRSTMRKKFDIAMAGGQDHLKGKIFRIGHLGFVCDRDILSCIGALEATL 360
           AVAP+ V AE IRS  +K FDI +AGGQD LKGKIFRIGHLGFV  RD+L+ I A+EA L
Sbjct: 300 AVAPVEVAAEDIRSFTKKHFDILLAGGQDDLKGKIFRIGHLGFVSGRDVLTAIAAIEAAL 359

Query: 361 IELGYEGVTPGSGVAAAAGVLAK 383
             LGY   T G+GVAAAA  LAK
Sbjct: 360 TGLGYSNFTSGAGVAAAAAELAK 382


Lambda     K      H
   0.317    0.134    0.386 

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: 433
Number of extensions: 11
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: 384
Length of database: 382
Length adjustment: 30
Effective length of query: 354
Effective length of database: 352
Effective search space:   124608
Effective search space used:   124608
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 (21.7 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