Align 4-guanidinobutyraldehyde dehydrogenase (EC 1.2.1.54) (characterized)
to candidate WP_040474635.1 MDG893_RS14400 aldehyde dehydrogenase
Query= metacyc::MONOMER-11560 (497 letters) >NCBI__GCF_000170835.1:WP_040474635.1 Length = 509 Score = 722 bits (1863), Expect = 0.0 Identities = 346/496 (69%), Positives = 416/496 (83%) Query: 2 TTLTRADWEQRAQQLKIEGRAFINGEYTDAVSGETFECLSPVDGRFLAKVASCDLADANR 61 T ++ +W+ A L IEGRA++ G Y AV+GETF +SPV+GR LA+VASCD ADA++ Sbjct: 13 TPTSQPEWQAMADTLAIEGRAYVKGSYRWAVNGETFPSISPVNGRELAQVASCDKADADK 72 Query: 62 AVENARATFNSGVWSQLAPAKRKAKLIRFADLLRKNVEELALLETLDMGKPIGDSSSIDI 121 AV AR F G W +LAP KRKA LIRFA+L+ + +ELALL+TLDMGKPI + ++D+ Sbjct: 73 AVAIARKVFERGDWRELAPIKRKAVLIRFAELIEAHGDELALLDTLDMGKPISHARTVDV 132 Query: 122 PGAAQAIHWTAEAIDKVYDEVAPTPHDQLGLVTREPVGVVGAIVPWNFPLLMACWKLGPA 181 P A+AI WTAEAIDKVY E+APTPH+Q+G+++REP+GVV AIVPWNFP++MA WK+ PA Sbjct: 133 PATARAIRWTAEAIDKVYGELAPTPHNQIGMISREPMGVVAAIVPWNFPMIMAAWKIAPA 192 Query: 182 LATGNSVVLKPSEKSPLTAIRIAQLAIEAGIPAGVLNVLPGYGHTVGKALALHMDVDTLV 241 LATGNSV+LKPSEKSPLTAIR+A LA EAGIP GV NVLPG+GHTVGKALALHMDVD LV Sbjct: 193 LATGNSVILKPSEKSPLTAIRLAALATEAGIPDGVFNVLPGFGHTVGKALALHMDVDCLV 252 Query: 242 FTGSTKIAKQLMVYAGESNMKRIWLEAGGKSPNIVFADAPDLQAAAEAAASAIAFNQGEV 301 FTGST +AKQLMVYAG+SNMKR+WLEAGGKSPNIVFADAPDL+ AA AASAIAFNQGEV Sbjct: 253 FTGSTNVAKQLMVYAGQSNMKRVWLEAGGKSPNIVFADAPDLKKAAAEAASAIAFNQGEV 312 Query: 302 CTAGSRLLVERSIKDKFLPMVVEALKGWKPGNPLDPQTTVGALVDTQQMNTVLSYIEAGH 361 CTAGSRLLVE S++ +F+ ++ EALK W+PG+PLDP TT GA+VD Q++ ++ YI G Sbjct: 313 CTAGSRLLVEESVRTEFVGLIREALKTWRPGHPLDPATTCGAIVDQAQLDRIIDYIGIGQ 372 Query: 362 KDGAKLLAGGKRTLEETGGTYVEPTIFDGVTNAMRIAQEEIFGPVLSVIAFDTAEEAVAI 421 +GAKL+ GG+R + ETGG +V+PT+FDGV N MRIA EEIFGPVLSVI F TAEEA+ I Sbjct: 373 SEGAKLVEGGQRVMAETGGLFVQPTVFDGVNNRMRIASEEIFGPVLSVIGFTTAEEAIEI 432 Query: 422 ANDTPYGLAAGIWTSDISKAHKTARAVRAGSVWVNQYDGGDMTAPFGGFKQSGNGRDKSL 481 AND+ YGLAA +WTS+I+ AHK A+A+RAGSVW+N YDGGDMTAPFGGFKQSGNGRDKSL Sbjct: 433 ANDSIYGLAAAVWTSNINTAHKVAKALRAGSVWINHYDGGDMTAPFGGFKQSGNGRDKSL 492 Query: 482 HALEKYTELKATWIKL 497 HA +KYTELKATW+ L Sbjct: 493 HAFDKYTELKATWLVL 508 Lambda K H 0.316 0.132 0.390 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: 777 Number of extensions: 24 Number of successful extensions: 1 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: 497 Length of database: 509 Length adjustment: 34 Effective length of query: 463 Effective length of database: 475 Effective search space: 219925 Effective search space used: 219925 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: 52 (24.6 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
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:
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