GapMind for Amino acid biosynthesis

 

Alignments for a candidate for trpE in Hydrogenovibrio halophilus DSM 15072

Align Anthranilate synthase component 1; AS; ASI; EC 4.1.3.27 (uncharacterized)
to candidate WP_019895717.1 A377_RS0107825 hypothetical protein

Query= curated2:Q9XAZ0
         (491 letters)



>NCBI__GCF_000384235.1:WP_019895717.1
          Length = 485

 Score =  252 bits (643), Expect = 2e-71
 Identities = 153/375 (40%), Positives = 221/375 (58%), Gaps = 24/375 (6%)

Query: 111 SLPRFTGGLVGYFGYETIYNFEHFAHRLKNTTKADPLGTPDILLMLSQELAVIDNLSGKI 170
           SLP FTGG   YFGYE       FA  L+ +        P    +      +ID+ +G  
Sbjct: 125 SLP-FTGGWFVYFGYE-------FAQVLEPSLSLPASNLPLAKWVRIPSAILIDHQTGHG 176

Query: 171 HLVVYADPSQPDGYERARERLEDIRTQLRQSCAIPLSLGSKHTEAVSEFGEEP---FKAC 227
           +LV     ++P    R     +D++   R   ++P         AV+E  ++P   F   
Sbjct: 177 YLV-----AEPGFEHRLHTLYQDLQQVGRVETSVP-------EIAVAEIHQDPPQRFTQG 224

Query: 228 VNKIKDYIFAGDCMQVVPSQRMSMEFTDSPLA-LYRALRTLNPSPYLFYYDFGDFHIVGS 286
           V++IKDYI AGD  QV  S++  ++  ++    +YRALR  NP+P+  Y DFGD+ ++ S
Sbjct: 225 VDRIKDYILAGDVFQVNLSRQWEVDVKNASAPNVYRALRQANPAPFAAYADFGDWQVLSS 284

Query: 287 SPEILVRRERDDVIVRPIAGTRLRGKTPAEDLANEQDLLSDAKEIAEHVMLIDLGRNDVG 346
           SPE LV  + + V  RPIAGTR R     +DLA  ++L +  KE+AEH+MLIDL RND+G
Sbjct: 285 SPERLVTSDGEHVATRPIAGTRRRSSDTEKDLALIRELQAHPKEVAEHIMLIDLERNDLG 344

Query: 347 RISKTGEVKVTDKMVIEKYSHVMHIVSNVEGRLKDGMTNMDILAATFPAGTLSGAPKVRA 406
           R+S+ G V V + M IE Y +V HIVSN++GRL+ G + +DI AATFP GT++G PK+R 
Sbjct: 345 RLSQPGSVAVDELMAIETYQYVHHIVSNIQGRLQPGTSPLDIFAATFPGGTITGCPKIRC 404

Query: 407 MEIIEEVEPSKRGIYGGAVGVWGFNNDMDLAIAIRTAVVKNNTLYVQSGAGVVADSDPAS 466
           MEII E+E + R  Y G++G    +  +D  I IRT V +   L  ++GAG+VADSDP  
Sbjct: 405 MEIIAELEQTPREAYTGSLGYINRDGRLDSNILIRTFVQQGERLRFRAGAGIVADSDPEK 464

Query: 467 EWQETQNKARAVIRA 481
           E  ET++KA+ +++A
Sbjct: 465 ELAETRHKAKGLLKA 479


Lambda     K      H
   0.318    0.136    0.396 

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: 630
Number of extensions: 35
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 2
Number of HSP's successfully gapped: 1
Length of query: 491
Length of database: 485
Length adjustment: 34
Effective length of query: 457
Effective length of database: 451
Effective search space:   206107
Effective search space used:   206107
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: 52 (24.6 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