GapMind for Amino acid biosynthesis

 

Alignments for a candidate for lysJ in Sulfurihydrogenibium azorense Az-Fu1

Align [LysW]-aminoadipate semialdehyde/glutamate semialdehyde transaminase; EC 2.6.1.118; EC 2.6.1.124 (uncharacterized)
to candidate WP_012673760.1 SULAZ_RS04620 glutamate-1-semialdehyde 2,1-aminomutase

Query= curated2:Q7SI94
         (388 letters)



>NCBI__GCF_000021545.1:WP_012673760.1
          Length = 427

 Score =  144 bits (362), Expect = 6e-39
 Identities = 109/329 (33%), Positives = 160/329 (48%), Gaps = 20/329 (6%)

Query: 13  IKIIKGEGQYVWDEKNNKYLDMHAGHGVAFLGHRNKVIIDHLKKQMEEISTLSLAFDTPI 72
           I I +G+G  +WD   N+Y+D     G   LGH +  +++ +K Q+    T S    T +
Sbjct: 36  IFIQRGKGSRIWDVDGNEYIDYVLSWGPLILGHAHDQVVNAIK-QVANYGT-SFGAPTEL 93

Query: 73  REEMIKEL-DELKPEDLDNLFLLNSGSEAVELALKIARKITKRRKIVAFKNSFHGR---- 127
             EM K + D +K  ++  +  +NSG+EA   A+++AR  TKR+KIV F   +HG     
Sbjct: 94  EIEMAKAVVDAVKSVEM--VRFVNSGTEATMSAIRLARGYTKRKKIVKFDGCYHGHGDSL 151

Query: 128 --SMGALSVTWNKKYREPF-EPLIGPVEFLEYNNVDSL----KSITEDTAAVIVEPVQGE 180
             S G+   T          E L      L YN+++++    K   ED A VI+EPV G 
Sbjct: 152 LVSAGSGVATLGIPGTPGIPEELANLTIVLPYNDIEAVEEAFKRYGEDIACVIIEPVAGN 211

Query: 181 GGVIPAKKEFVKSLREVTEKVNALLIIDEVQTGFGRTGKIWAYQHFDIKPDILTAGKAIG 240
            GV+   KE+ + LR++T K  ALLI DEV TGF R     A + + I PD+ T GK IG
Sbjct: 212 MGVVAPSKEYHQRLRDITRKYGALLIFDEVMTGF-RLAYGGAQELYGIDPDLTTFGKVIG 270

Query: 241 GGFPVSAVFLPNWISEKIEEGD---HGSTYGGNPLAAAAVTAACKVAKSEKIAEQAQKKG 297
           GG PV A      I E +          T  GNPLA AA     ++ K      +  +KG
Sbjct: 271 GGLPVGAYGGKREIMEYVAPVGPVYQAGTLSGNPLAMAAGLRQLQLLKELNPYRELDEKG 330

Query: 298 ELFMRILKEKLEDFKIVREIRGLGLMIGI 326
                  K+  ++F    ++  +G MI +
Sbjct: 331 RFLEEGFKQIAQEFSAAIQVNRVGSMITV 359


Lambda     K      H
   0.317    0.136    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: 398
Number of extensions: 16
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: 388
Length of database: 427
Length adjustment: 31
Effective length of query: 357
Effective length of database: 396
Effective search space:   141372
Effective search space used:   141372
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 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Apr 10 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