GapMind for catabolism of small carbon sources

 

Alignments for a candidate for glucosaminate-lyase in Herbaspirillum seropedicae SmR1

Align D-glucosaminate dehydratase (EC 4.3.1.9) (characterized)
to candidate HSERO_RS08720 HSERO_RS08720 amino acid deaminase

Query= reanno::pseudo5_N2C3_1:AO356_00450
         (405 letters)



>FitnessBrowser__HerbieS:HSERO_RS08720
          Length = 430

 Score =  377 bits (967), Expect = e-109
 Identities = 204/406 (50%), Positives = 266/406 (65%), Gaps = 5/406 (1%)

Query: 5   IPNAGVEKGAATVGAHLL-KDVSLPALVLHRAALEHNIRWMQAFVTDSGAELAPHGKTSM 63
           +P A     A TV  +LL +D+SLPA VL+   + HN++WMQ FV     +LAPHGKT+M
Sbjct: 25  LPQALPPGQAGTVRWNLLNEDISLPAAVLYEEKIAHNLKWMQEFVGQYQLKLAPHGKTTM 84

Query: 64  TPALFRRQLDAGAWGLTLATAVQTRAAYAHGVRRVLMANQLVGTPNMALIADLLADPAFE 123
            P LF RQLD GAWG+TLATA QT A Y HGVRRV+MANQLVG  NMA+I++LLADP+FE
Sbjct: 85  APKLFARQLDTGAWGITLATAHQTLAGYHHGVRRVIMANQLVGKRNMAIISELLADPSFE 144

Query: 124 FHCMVDHPDNVADLGAFFASRGMKLNVMIEYGVVGGRCGCRTEAEVLALAEAIRSQPALA 183
           F C+VD    V  LG FFA R   LNV++E G  GGR G R EA+  A+ EAI    ++A
Sbjct: 145 FFCLVDSAALVDQLGRFFAERKQTLNVLLELGPTGGRTGVRDEAQQQAVLEAISRWDSIA 204

Query: 184 LTGIEGYEGVIHGDHAISG-IRAFAASLVRLAVQLQDDDAFAIDKPIITASGSAWYDLIA 242
           L G+E YEGV+  +  I   ++   A L  LA Q Q     A    ++T +GSAWYD++A
Sbjct: 205 LAGVEVYEGVLKEEVDIRRFLQRAVACLQDLAAQGQLARRLARGPAVLTGAGSAWYDVVA 264

Query: 243 ESFEAQNAHGRFLSVLRPGSYVAHDHGIYKEAQCCVLERRSDLH---EGLRPALEVWAHV 299
           E F   +       VLRPG Y+ HD GIY+ AQ  +  R    H     L+PAL++WA+V
Sbjct: 265 EEFGQADIGAALDVVLRPGCYLTHDVGIYRAAQAQIQVRNPVAHSMRSQLQPALQLWAYV 324

Query: 300 QSLPEPGFAVIALGKRDVAYDAGLPVPLKRYTPGSDSVPGDDVSGCKVTAVMDQHAFMSV 359
           QS+PE   A+IALGKRD A+DAGLP+P+ R+ PG D+ P    +  +VT +MDQHA++ +
Sbjct: 325 QSIPESDKAIIALGKRDAAFDAGLPMPVSRFRPGRDTGPQATPAHWEVTGMMDQHAYLKI 384

Query: 360 AAGVELRVGDIIAFGTSHPCLTFDKWRVGCLVDEQLRVVESMETCF 405
           AAG ++ VGD+IAF  SHPCLTFDKWR   +VD +  V + ++T F
Sbjct: 385 AAGDDIEVGDMIAFDISHPCLTFDKWRHLVVVDGRFDVTDIVQTFF 430


Lambda     K      H
   0.322    0.136    0.414 

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: 509
Number of extensions: 16
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: 405
Length of database: 430
Length adjustment: 32
Effective length of query: 373
Effective length of database: 398
Effective search space:   148454
Effective search space used:   148454
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: 50 (23.9 bits)

This GapMind analysis is from Sep 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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