GapMind for Amino acid biosynthesis

 

Alignments for a candidate for asnB in Methylomicrobium alcaliphilum 20Z

Align Putative asparagine synthetase [glutamine-hydrolyzing] 2; EC 6.3.5.4 (uncharacterized)
to candidate WP_014149127.1 MEALZ_RS13110 asparagine synthase

Query= curated2:Q58456
         (515 letters)



>NCBI__GCF_000968535.2:WP_014149127.1
          Length = 599

 Score =  153 bits (387), Expect = 1e-41
 Identities = 109/376 (28%), Positives = 179/376 (47%), Gaps = 30/376 (7%)

Query: 44  YSIGLGHVRLAILDLSEKGHQP------MGYNVDEDKIIYRDDE--LDRADIIIVYNGEI 95
           Y  G+   + + L  S KG  P      +G  + E   +  DD+  L++ D  +   G  
Sbjct: 8   YGTGIDRNQASELAESLKGCAPESTKKTIGIRIAESLALVSDDKRSLEQGDCRLALTGHG 67

Query: 96  YNYLELKEKFNLETETGTDTEVILKLYNKLGFDCVKEFNGMWAFCIFDKKKGLIFCSRDR 155
           +  LE                 I++ Y   G D +K+  G +   +FD+ +  +  + DR
Sbjct: 68  FGPLE----------------AIVENYKTKGDDFIKDMQGAFTLMLFDEYEKRLLLATDR 111

Query: 156 LGVKPFYYYWDGNEFIFSSELKGILAVKEINKKENINKDAVELYFALGFIPSPYSIYKNT 215
           LG    YY    N  +F S    ++A  E++ +  I++ ++  Y      PSP++IY+  
Sbjct: 112 LGQNNLYYAQTLNGIVFGSTADSVVAHPEVSSE--ISRQSIYDYVYFHHCPSPHTIYRQV 169

Query: 216 FKLEARQNLIFDLDKREIRKYYYWELPDYKPIYDKKKLIEEGKKLLYDAVKIRMRSDVPV 275
            KLE  Q L +  D +   +YY+  +   +  Y  ++  +E +  + +AV+         
Sbjct: 170 QKLEGGQVLTYQ-DGKIALQYYWMPVFSEQGAYSLEQSGQELRNEIIEAVRQSAADSNVT 228

Query: 276 GAFLSGGLDSSTVVGVMRE-FTDLSKLHTFSIGFEGKYDETPYIKIVVDYFKTQHHHYYF 334
           GAFLSGGLDSS+V G + + + + +K  T     EG YDE  Y +I VD FKT+ H YY 
Sbjct: 229 GAFLSGGLDSSSVAGALSKVYPEQAKTFTMGFPVEG-YDEIEYARIAVDCFKTRPHEYYV 287

Query: 335 KERDFEELIDKYSWIYDEPFGDYSGFPTYKVSEMARK-FVTVVLSGDGGDEVFGGYMTHL 393
              D    + K +  YDEPFG+ S    Y  +++A++  + V+L+GDGGDE+F G   + 
Sbjct: 288 TPEDTVAAVPKIAAFYDEPFGNSSALAAYYCAKLAKENGIQVMLAGDGGDELFAGNERYA 347

Query: 394 NGYRMDFIRKLPKFLR 409
                D   ++P F R
Sbjct: 348 KQLLFDRYYRIPGFAR 363


Lambda     K      H
   0.322    0.144    0.434 

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: 801
Number of extensions: 44
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: 515
Length of database: 599
Length adjustment: 36
Effective length of query: 479
Effective length of database: 563
Effective search space:   269677
Effective search space used:   269677
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 (21.9 bits)
S2: 53 (25.0 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