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: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 8 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4Q0K7
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 2 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003723 | RNA binding | 4 | 2 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0016301 | kinase activity | 4 | 2 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 382 | 384 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.493 |
CLV_PCSK_FUR_1 | 330 | 334 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 381 | 383 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.455 |
CLV_PCSK_PC7_1 | 98 | 104 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 98 | 102 | PF00082 | 0.461 |
DEG_APCC_DBOX_1 | 175 | 183 | PF00400 | 0.392 |
DEG_APCC_DBOX_1 | 312 | 320 | PF00400 | 0.448 |
DOC_CKS1_1 | 187 | 192 | PF01111 | 0.384 |
DOC_CYCLIN_RxL_1 | 98 | 110 | PF00134 | 0.438 |
DOC_MAPK_gen_1 | 406 | 415 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 98 | 107 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 176 | 183 | PF00069 | 0.389 |
DOC_MAPK_MEF2A_6 | 186 | 195 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 409 | 417 | PF00069 | 0.433 |
DOC_PP4_FxxP_1 | 187 | 190 | PF00568 | 0.488 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 26 | 30 | PF00917 | 0.463 |
DOC_WW_Pin1_4 | 186 | 191 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.636 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.455 |
LIG_14-3-3_CanoR_1 | 214 | 222 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 400 | 410 | PF00244 | 0.540 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.740 |
LIG_BIR_III_2 | 369 | 373 | PF00653 | 0.416 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.629 |
LIG_CSL_BTD_1 | 217 | 220 | PF09270 | 0.474 |
LIG_deltaCOP1_diTrp_1 | 253 | 263 | PF00928 | 0.321 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.529 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.348 |
LIG_FHA_1 | 410 | 416 | PF00498 | 0.621 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.440 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.527 |
LIG_HCF-1_HBM_1 | 232 | 235 | PF13415 | 0.490 |
LIG_LIR_Apic_2 | 184 | 190 | PF02991 | 0.473 |
LIG_LIR_Apic_2 | 216 | 221 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 146 | 151 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 260 | 266 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 439 | 444 | PF02991 | 0.379 |
LIG_Pex14_2 | 183 | 187 | PF04695 | 0.373 |
LIG_Rb_pABgroove_1 | 225 | 233 | PF01858 | 0.463 |
LIG_SH2_NCK_1 | 235 | 239 | PF00017 | 0.520 |
LIG_SH2_STAP1 | 341 | 345 | PF00017 | 0.314 |
LIG_SH2_STAT3 | 160 | 163 | PF00017 | 0.514 |
LIG_SH2_STAT3 | 341 | 344 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.469 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.657 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.529 |
LIG_SUMO_SIM_anti_2 | 414 | 420 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 103 | 108 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 178 | 184 | PF11976 | 0.351 |
LIG_SUMO_SIM_par_1 | 411 | 416 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 62 | 67 | PF11976 | 0.433 |
LIG_SxIP_EBH_1 | 16 | 28 | PF03271 | 0.397 |
LIG_TRAF2_1 | 303 | 306 | PF00917 | 0.387 |
MOD_CDK_SPK_2 | 90 | 95 | PF00069 | 0.475 |
MOD_CDK_SPxK_1 | 370 | 376 | PF00069 | 0.528 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.616 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.542 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.489 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.738 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.506 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.618 |
MOD_CMANNOS | 251 | 254 | PF00535 | 0.530 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.465 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.417 |
MOD_GlcNHglycan | 206 | 210 | PF01048 | 0.621 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.584 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.610 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.487 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.678 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.434 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.521 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.653 |
MOD_LATS_1 | 407 | 413 | PF00433 | 0.506 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.496 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.424 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.399 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.493 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.586 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.484 |
MOD_PIKK_1 | 105 | 111 | PF00454 | 0.487 |
MOD_PIKK_1 | 162 | 168 | PF00454 | 0.536 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.511 |
MOD_PIKK_1 | 267 | 273 | PF00454 | 0.561 |
MOD_PIKK_1 | 389 | 395 | PF00454 | 0.303 |
MOD_PKA_1 | 98 | 104 | PF00069 | 0.326 |
MOD_PKA_2 | 213 | 219 | PF00069 | 0.561 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.495 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.326 |
MOD_Plk_1 | 158 | 164 | PF00069 | 0.563 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.498 |
MOD_Plk_2-3 | 411 | 417 | PF00069 | 0.435 |
MOD_Plk_2-3 | 74 | 80 | PF00069 | 0.480 |
MOD_Plk_4 | 27 | 33 | PF00069 | 0.474 |
MOD_Plk_4 | 425 | 431 | PF00069 | 0.423 |
MOD_ProDKin_1 | 186 | 192 | PF00069 | 0.377 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.597 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.623 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.443 |
MOD_SUMO_for_1 | 387 | 390 | PF00179 | 0.517 |
MOD_SUMO_for_1 | 405 | 408 | PF00179 | 0.484 |
MOD_SUMO_rev_2 | 86 | 93 | PF00179 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 100 | 105 | PF01217 | 0.406 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.347 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.506 |
TRG_ER_diArg_1 | 313 | 316 | PF00400 | 0.556 |
TRG_ER_diArg_1 | 330 | 333 | PF00400 | 0.658 |
TRG_ER_diArg_1 | 380 | 383 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.524 |
TRG_Pf-PMV_PEXEL_1 | 102 | 106 | PF00026 | 0.435 |
TRG_Pf-PMV_PEXEL_1 | 153 | 158 | PF00026 | 0.367 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFJ4 | Leptomonas seymouri | 36% | 96% |
A0A1X0P061 | Trypanosomatidae | 23% | 100% |
A0A3Q8ILN7 | Leishmania donovani | 91% | 100% |
A0A422NKD5 | Trypanosoma rangeli | 26% | 100% |
A4HQ70 | Leishmania braziliensis | 71% | 98% |
A4IDW8 | Leishmania infantum | 92% | 100% |
E9ATY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 98% |
V5BNR2 | Trypanosoma cruzi | 27% | 100% |