Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 8 |
Pissara et al. | yes | yes: 32 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 20 |
GO:0110165 | cellular anatomical entity | 1 | 20 |
GO:0005654 | nucleoplasm | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 20 |
GO:0006807 | nitrogen compound metabolic process | 2 | 20 |
GO:0008152 | metabolic process | 1 | 20 |
GO:0019538 | protein metabolic process | 3 | 20 |
GO:0043170 | macromolecule metabolic process | 3 | 20 |
GO:0044238 | primary metabolic process | 2 | 20 |
GO:0071704 | organic substance metabolic process | 2 | 20 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 20 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 20 |
GO:0004177 | aminopeptidase activity | 5 | 20 |
GO:0005488 | binding | 1 | 20 |
GO:0008233 | peptidase activity | 3 | 20 |
GO:0008235 | metalloexopeptidase activity | 5 | 20 |
GO:0008237 | metallopeptidase activity | 4 | 20 |
GO:0008238 | exopeptidase activity | 4 | 20 |
GO:0016787 | hydrolase activity | 2 | 20 |
GO:0030145 | manganese ion binding | 6 | 20 |
GO:0043167 | ion binding | 2 | 20 |
GO:0043169 | cation binding | 3 | 20 |
GO:0046872 | metal ion binding | 4 | 20 |
GO:0046914 | transition metal ion binding | 5 | 20 |
GO:0070006 | metalloaminopeptidase activity | 6 | 20 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 20 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_KEX2_1 | 170 | 172 | PF00082 | 0.351 |
CLV_PCSK_KEX2_1 | 431 | 433 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.615 |
CLV_PCSK_PC1ET2_1 | 170 | 172 | PF00082 | 0.384 |
CLV_PCSK_PC1ET2_1 | 431 | 433 | PF00082 | 0.457 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.615 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 380 | 384 | PF00082 | 0.347 |
DOC_CYCLIN_yCln2_LP_2 | 334 | 340 | PF00134 | 0.312 |
DOC_CYCLIN_yCln2_LP_2 | 443 | 449 | PF00134 | 0.369 |
DOC_MAPK_gen_1 | 363 | 372 | PF00069 | 0.347 |
DOC_MAPK_gen_1 | 46 | 56 | PF00069 | 0.381 |
DOC_MAPK_MEF2A_6 | 363 | 372 | PF00069 | 0.401 |
DOC_MAPK_MEF2A_6 | 94 | 103 | PF00069 | 0.475 |
DOC_PP1_RVXF_1 | 286 | 292 | PF00149 | 0.246 |
DOC_PP2B_LxvP_1 | 334 | 337 | PF13499 | 0.391 |
DOC_PP2B_LxvP_1 | 501 | 504 | PF13499 | 0.431 |
DOC_PP2B_PxIxI_1 | 397 | 403 | PF00149 | 0.401 |
DOC_PP4_FxxP_1 | 453 | 456 | PF00568 | 0.294 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.214 |
DOC_USP7_MATH_1 | 475 | 479 | PF00917 | 0.346 |
DOC_USP7_MATH_2 | 337 | 343 | PF00917 | 0.345 |
DOC_USP7_UBL2_3 | 466 | 470 | PF12436 | 0.405 |
DOC_WW_Pin1_4 | 281 | 286 | PF00397 | 0.347 |
DOC_WW_Pin1_4 | 394 | 399 | PF00397 | 0.329 |
LIG_14-3-3_CanoR_1 | 49 | 54 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 94 | 100 | PF00244 | 0.467 |
LIG_Actin_WH2_2 | 219 | 237 | PF00022 | 0.468 |
LIG_Actin_WH2_2 | 47 | 65 | PF00022 | 0.286 |
LIG_APCC_ABBA_1 | 70 | 75 | PF00400 | 0.290 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.584 |
LIG_BIR_III_4 | 376 | 380 | PF00653 | 0.347 |
LIG_CaM_NSCaTE_8 | 230 | 237 | PF13499 | 0.356 |
LIG_CtBP_PxDLS_1 | 248 | 254 | PF00389 | 0.382 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.536 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.327 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.356 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.345 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.299 |
LIG_FHA_1 | 395 | 401 | PF00498 | 0.312 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.391 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.410 |
LIG_FHA_2 | 220 | 226 | PF00498 | 0.299 |
LIG_FHA_2 | 373 | 379 | PF00498 | 0.347 |
LIG_FHA_2 | 504 | 510 | PF00498 | 0.431 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.517 |
LIG_LIR_Apic_2 | 452 | 456 | PF02991 | 0.351 |
LIG_LIR_Gen_1 | 220 | 231 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 457 | 465 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 495 | 504 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.677 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 33 | 37 | PF02991 | 0.499 |
LIG_LIR_Nem_3 | 442 | 448 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 457 | 462 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 495 | 499 | PF02991 | 0.319 |
LIG_PCNA_yPIPBox_3 | 233 | 246 | PF02747 | 0.214 |
LIG_PDZ_Class_3 | 522 | 527 | PF00595 | 0.522 |
LIG_PTB_Apo_2 | 452 | 459 | PF02174 | 0.422 |
LIG_SH2_CRK | 256 | 260 | PF00017 | 0.356 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.549 |
LIG_SH2_CRK | 459 | 463 | PF00017 | 0.348 |
LIG_SH2_GRB2like | 178 | 181 | PF00017 | 0.503 |
LIG_SH2_GRB2like | 423 | 426 | PF00017 | 0.358 |
LIG_SH2_NCK_1 | 459 | 463 | PF00017 | 0.214 |
LIG_SH2_NCK_1 | 74 | 78 | PF00017 | 0.468 |
LIG_SH2_SRC | 178 | 181 | PF00017 | 0.503 |
LIG_SH2_STAP1 | 459 | 463 | PF00017 | 0.214 |
LIG_SH2_STAP1 | 74 | 78 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 35 | 38 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.388 |
LIG_SH3_3 | 113 | 119 | PF00018 | 0.212 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.347 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.411 |
LIG_SUMO_SIM_anti_2 | 196 | 201 | PF11976 | 0.305 |
LIG_SUMO_SIM_anti_2 | 52 | 59 | PF11976 | 0.363 |
LIG_SUMO_SIM_par_1 | 186 | 191 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 271 | 276 | PF11976 | 0.318 |
LIG_SUMO_SIM_par_1 | 52 | 59 | PF11976 | 0.398 |
LIG_TRAF2_1 | 12 | 15 | PF00917 | 0.578 |
LIG_TRAF2_1 | 247 | 250 | PF00917 | 0.431 |
LIG_UBA3_1 | 361 | 365 | PF00899 | 0.342 |
MOD_CDK_SPK_2 | 281 | 286 | PF00069 | 0.405 |
MOD_CDK_SPxxK_3 | 281 | 288 | PF00069 | 0.347 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.372 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.334 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.468 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.503 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.347 |
MOD_CK1_1 | 468 | 474 | PF00069 | 0.419 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.298 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.347 |
MOD_CK2_1 | 503 | 509 | PF00069 | 0.377 |
MOD_CK2_1 | 8 | 14 | PF00069 | 0.546 |
MOD_CK2_1 | 81 | 87 | PF00069 | 0.478 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.577 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.440 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.542 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.347 |
MOD_GlcNHglycan | 435 | 438 | PF01048 | 0.362 |
MOD_GlcNHglycan | 459 | 462 | PF01048 | 0.494 |
MOD_GlcNHglycan | 64 | 68 | PF01048 | 0.342 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.427 |
MOD_GSK3_1 | 217 | 224 | PF00069 | 0.318 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.340 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.494 |
MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.439 |
MOD_N-GLC_1 | 163 | 168 | PF02516 | 0.218 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.477 |
MOD_N-GLC_1 | 372 | 377 | PF02516 | 0.307 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.357 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.347 |
MOD_NEK2_1 | 259 | 264 | PF00069 | 0.334 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.282 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.331 |
MOD_NEK2_2 | 310 | 315 | PF00069 | 0.418 |
MOD_NEK2_2 | 465 | 470 | PF00069 | 0.446 |
MOD_PIKK_1 | 352 | 358 | PF00454 | 0.361 |
MOD_PK_1 | 105 | 111 | PF00069 | 0.501 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.377 |
MOD_PKB_1 | 6 | 14 | PF00069 | 0.566 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.452 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.460 |
MOD_Plk_1 | 163 | 169 | PF00069 | 0.283 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.494 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.394 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.464 |
MOD_Plk_1 | 392 | 398 | PF00069 | 0.401 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.540 |
MOD_Plk_2-3 | 219 | 225 | PF00069 | 0.342 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.459 |
MOD_Plk_4 | 30 | 36 | PF00069 | 0.358 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.377 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.356 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.403 |
MOD_ProDKin_1 | 281 | 287 | PF00069 | 0.347 |
MOD_ProDKin_1 | 394 | 400 | PF00069 | 0.329 |
MOD_SUMO_rev_2 | 460 | 468 | PF00179 | 0.290 |
TRG_DiLeu_BaLyEn_6 | 97 | 102 | PF01217 | 0.468 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.657 |
TRG_ENDOCYTIC_2 | 459 | 462 | PF00928 | 0.256 |
TRG_ER_FFAT_2 | 452 | 464 | PF00635 | 0.372 |
TRG_NES_CRM1_1 | 359 | 371 | PF08389 | 0.401 |
TRG_NLS_MonoExtC_3 | 169 | 175 | PF00514 | 0.312 |
TRG_NLS_MonoExtC_3 | 4 | 10 | PF00514 | 0.595 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6B6 | Leptomonas seymouri | 32% | 97% |
A0A0N0P8E6 | Leptomonas seymouri | 79% | 100% |
A0A0N1PAS4 | Leptomonas seymouri | 43% | 98% |
A0A0S4IQ79 | Bodo saltans | 54% | 100% |
A0A1X0NWR5 | Trypanosomatidae | 49% | 100% |
A0A1X0P4M9 | Trypanosomatidae | 48% | 100% |
A0A3R7JY84 | Trypanosoma rangeli | 48% | 100% |
A0A3R7N130 | Trypanosoma rangeli | 56% | 94% |
A0A3S7WRP1 | Leishmania donovani | 44% | 99% |
A0A3S7X742 | Leishmania donovani | 86% | 100% |
A0K9N9 | Burkholderia cenocepacia (strain HI2424) | 29% | 100% |
A0KPF3 | Aeromonas hydrophila subsp. hydrophila (strain ATCC 7966 / DSM 30187 / BCRC 13018 / CCUG 14551 / JCM 1027 / KCTC 2358 / NCIMB 9240 / NCTC 8049) | 31% | 100% |
A1SRZ1 | Psychromonas ingrahamii (strain 37) | 29% | 100% |
A3QBG2 | Shewanella loihica (strain ATCC BAA-1088 / PV-4) | 29% | 100% |
A4H6I8 | Leishmania braziliensis | 43% | 97% |
A4HCW4 | Leishmania braziliensis | 32% | 100% |
A4HUX3 | Leishmania infantum | 44% | 99% |
A4I996 | Leishmania infantum | 86% | 100% |
A4SSA7 | Aeromonas salmonicida (strain A449) | 31% | 100% |
A5GV03 | Synechococcus sp. (strain RCC307) | 30% | 100% |
A6U7J2 | Sinorhizobium medicae (strain WSM419) | 34% | 100% |
A8LI79 | Dinoroseobacter shibae (strain DSM 16493 / NCIMB 14021 / DFL 12) | 32% | 100% |
A9AHG9 | Burkholderia multivorans (strain ATCC 17616 / 249) | 27% | 100% |
A9BBV5 | Prochlorococcus marinus (strain MIT 9211) | 29% | 100% |
B0CCF6 | Acaryochloris marina (strain MBIC 11017) | 29% | 100% |
B0U1L5 | Xylella fastidiosa (strain M12) | 28% | 100% |
B1JWV2 | Burkholderia cenocepacia (strain MC0-3) | 29% | 100% |
B1XK83 | Synechococcus sp. (strain ATCC 27264 / PCC 7002 / PR-6) | 30% | 100% |
B2I6L3 | Xylella fastidiosa (strain M23) | 27% | 100% |
B2J3G8 | Nostoc punctiforme (strain ATCC 29133 / PCC 73102) | 32% | 100% |
B2T146 | Paraburkholderia phytofirmans (strain DSM 17436 / LMG 22146 / PsJN) | 28% | 100% |
B2UAK8 | Ralstonia pickettii (strain 12J) | 29% | 100% |
B4F2N1 | Proteus mirabilis (strain HI4320) | 29% | 100% |
B5F9Q6 | Aliivibrio fischeri (strain MJ11) | 29% | 100% |
B5ZWY7 | Rhizobium leguminosarum bv. trifolii (strain WSM2304) | 33% | 100% |
B8CU18 | Shewanella piezotolerans (strain WP3 / JCM 13877) | 28% | 100% |
B8GTX6 | Thioalkalivibrio sulfidiphilus (strain HL-EbGR7) | 29% | 100% |
B8HTK3 | Cyanothece sp. (strain PCC 7425 / ATCC 29141) | 29% | 100% |
B9JCD8 | Agrobacterium radiobacter (strain K84 / ATCC BAA-868) | 35% | 100% |
C0QC86 | Desulforapulum autotrophicum (strain ATCC 43914 / DSM 3382 / VKM B-1955 / HRM2) | 29% | 100% |
C3M9C8 | Sinorhizobium fredii (strain NBRC 101917 / NGR234) | 33% | 100% |
C4LA51 | Tolumonas auensis (strain DSM 9187 / TA4) | 29% | 100% |
C5CCM4 | Micrococcus luteus (strain ATCC 4698 / DSM 20030 / JCM 1464 / NBRC 3333 / NCIMB 9278 / NCTC 2665 / VKM Ac-2230) | 33% | 100% |
C9ZV91 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 79% |
D0A654 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 93% |
D0A7H3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9ANK8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 99% |
E9B496 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
O06865 | Synechococcus elongatus (strain PCC 7942 / FACHB-805) | 31% | 100% |
P34629 | Caenorhabditis elegans | 36% | 100% |
Q086N8 | Shewanella frigidimarina (strain NCIMB 400) | 27% | 100% |
Q0BCQ2 | Burkholderia ambifaria (strain ATCC BAA-244 / AMMD) | 29% | 100% |
Q11A96 | Trichodesmium erythraeum (strain IMS101) | 30% | 100% |
Q12QW7 | Shewanella denitrificans (strain OS217 / ATCC BAA-1090 / DSM 15013) | 28% | 100% |
Q1BUE7 | Burkholderia cenocepacia (strain AU 1054) | 29% | 100% |
Q215R8 | Rhodopseudomonas palustris (strain BisB18) | 33% | 100% |
Q39DS5 | Burkholderia lata (strain ATCC 17760 / DSM 23089 / LMG 22485 / NCIMB 9086 / R18194 / 383) | 29% | 100% |
Q3M9J6 | Trichormus variabilis (strain ATCC 29413 / PCC 7937) | 31% | 100% |
Q488M4 | Colwellia psychrerythraea (strain 34H / ATCC BAA-681) | 28% | 100% |
Q4Q3T0 | Leishmania major | 85% | 100% |
Q4QH17 | Leishmania major | 44% | 99% |
Q5E7T8 | Aliivibrio fischeri (strain ATCC 700601 / ES114) | 29% | 100% |
Q5N569 | Synechococcus sp. (strain ATCC 27144 / PCC 6301 / SAUG 1402/1) | 31% | 100% |
Q5QY05 | Idiomarina loihiensis (strain ATCC BAA-735 / DSM 15497 / L2-TR) | 29% | 100% |
Q5R7G6 | Pongo abelii | 43% | 100% |
Q6LUW0 | Photobacterium profundum (strain SS9) | 29% | 100% |
Q6NSR8 | Mus musculus | 44% | 100% |
Q7M8W6 | Wolinella succinogenes (strain ATCC 29543 / DSM 1740 / LMG 7466 / NCTC 11488 / FDC 602W) | 32% | 100% |
Q7VAP4 | Prochlorococcus marinus (strain SARG / CCMP1375 / SS120) | 31% | 100% |
Q87F32 | Xylella fastidiosa (strain Temecula1 / ATCC 700964) | 27% | 100% |
Q8K9I0 | Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) | 28% | 100% |
Q8NDH3 | Homo sapiens | 43% | 100% |
Q8Z064 | Nostoc sp. (strain PCC 7120 / SAG 25.82 / UTEX 2576) | 31% | 100% |
Q92QY7 | Rhizobium meliloti (strain 1021) | 35% | 100% |
Q9PH08 | Xylella fastidiosa (strain 9a5c) | 27% | 100% |
Q9Y935 | Aeropyrum pernix (strain ATCC 700893 / DSM 11879 / JCM 9820 / NBRC 100138 / K1) | 27% | 100% |
V5BTR1 | Trypanosoma cruzi | 56% | 95% |
V5BWE3 | Trypanosoma cruzi | 50% | 100% |