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: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HDV8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.675 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 270 | 272 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.383 |
CLV_PCSK_PC1ET2_1 | 379 | 381 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 372 | 376 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 402 | 406 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.339 |
DEG_APCC_DBOX_1 | 62 | 70 | PF00400 | 0.377 |
DEG_COP1_1 | 253 | 262 | PF00400 | 0.525 |
DOC_CKS1_1 | 192 | 197 | PF01111 | 0.390 |
DOC_CKS1_1 | 299 | 304 | PF01111 | 0.521 |
DOC_CYCLIN_RxL_1 | 309 | 320 | PF00134 | 0.263 |
DOC_MAPK_gen_1 | 13 | 21 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 151 | 160 | PF00069 | 0.621 |
DOC_MAPK_gen_1 | 379 | 387 | PF00069 | 0.356 |
DOC_MAPK_gen_1 | 397 | 407 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 15 | 23 | PF00069 | 0.321 |
DOC_MAPK_MEF2A_6 | 154 | 162 | PF00069 | 0.477 |
DOC_MAPK_MEF2A_6 | 400 | 407 | PF00069 | 0.305 |
DOC_PP4_FxxP_1 | 299 | 302 | PF00568 | 0.387 |
DOC_PP4_FxxP_1 | 383 | 386 | PF00568 | 0.375 |
DOC_PP4_FxxP_1 | 70 | 73 | PF00568 | 0.294 |
DOC_USP7_MATH_1 | 145 | 149 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.713 |
DOC_USP7_MATH_2 | 442 | 448 | PF00917 | 0.493 |
DOC_WW_Pin1_4 | 191 | 196 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.560 |
DOC_WW_Pin1_4 | 452 | 457 | PF00397 | 0.471 |
LIG_14-3-3_CanoR_1 | 102 | 109 | PF00244 | 0.381 |
LIG_14-3-3_CanoR_1 | 15 | 20 | PF00244 | 0.257 |
LIG_14-3-3_CanoR_1 | 173 | 182 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 270 | 276 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 36 | 45 | PF00244 | 0.283 |
LIG_14-3-3_CanoR_1 | 414 | 420 | PF00244 | 0.432 |
LIG_AP2alpha_2 | 438 | 440 | PF02296 | 0.497 |
LIG_APCC_ABBA_1 | 200 | 205 | PF00400 | 0.383 |
LIG_BRCT_BRCA1_1 | 263 | 267 | PF00533 | 0.463 |
LIG_BRCT_BRCA1_1 | 3 | 7 | PF00533 | 0.373 |
LIG_deltaCOP1_diTrp_1 | 54 | 60 | PF00928 | 0.330 |
LIG_DLG_GKlike_1 | 15 | 22 | PF00625 | 0.413 |
LIG_FAT_LD_1 | 19 | 27 | PF03623 | 0.467 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.405 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.457 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.561 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.419 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.513 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.435 |
LIG_FHA_2 | 15 | 21 | PF00498 | 0.463 |
LIG_FHA_2 | 430 | 436 | PF00498 | 0.399 |
LIG_FHA_2 | 441 | 447 | PF00498 | 0.485 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.529 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.368 |
LIG_LIR_Apic_2 | 68 | 73 | PF02991 | 0.293 |
LIG_LIR_Gen_1 | 4 | 12 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 54 | 61 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 165 | 171 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 325 | 330 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 4 | 10 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 54 | 58 | PF02991 | 0.360 |
LIG_MYND_1 | 312 | 316 | PF01753 | 0.423 |
LIG_NRBOX | 18 | 24 | PF00104 | 0.412 |
LIG_PCNA_yPIPBox_3 | 228 | 242 | PF02747 | 0.377 |
LIG_PDZ_Class_1 | 452 | 457 | PF00595 | 0.471 |
LIG_Pex14_2 | 383 | 387 | PF04695 | 0.368 |
LIG_SH2_NCK_1 | 263 | 267 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 198 | 202 | PF00017 | 0.272 |
LIG_SH2_STAP1 | 263 | 267 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 377 | 381 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 130 | 133 | PF00017 | 0.383 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.332 |
LIG_SH3_1 | 201 | 207 | PF00018 | 0.410 |
LIG_SH3_1 | 313 | 319 | PF00018 | 0.247 |
LIG_SH3_3 | 189 | 195 | PF00018 | 0.393 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.460 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.441 |
LIG_SH3_3 | 313 | 319 | PF00018 | 0.322 |
LIG_SH3_3 | 436 | 442 | PF00018 | 0.487 |
LIG_SUMO_SIM_anti_2 | 17 | 23 | PF11976 | 0.461 |
LIG_SUMO_SIM_par_1 | 319 | 326 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 64 | 71 | PF11976 | 0.391 |
LIG_TRAF2_1 | 364 | 367 | PF00917 | 0.558 |
LIG_TRAF2_1 | 443 | 446 | PF00917 | 0.501 |
LIG_UBA3_1 | 84 | 91 | PF00899 | 0.375 |
MOD_CK1_1 | 39 | 45 | PF00069 | 0.430 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.439 |
MOD_CK2_1 | 14 | 20 | PF00069 | 0.303 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.665 |
MOD_CK2_1 | 429 | 435 | PF00069 | 0.353 |
MOD_CK2_1 | 440 | 446 | PF00069 | 0.476 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.294 |
MOD_Cter_Amidation | 30 | 33 | PF01082 | 0.399 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.513 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.585 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.523 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.288 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.456 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.420 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.526 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.414 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.512 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.678 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.387 |
MOD_LATS_1 | 268 | 274 | PF00433 | 0.570 |
MOD_N-GLC_1 | 173 | 178 | PF02516 | 0.477 |
MOD_N-GLC_2 | 357 | 359 | PF02516 | 0.434 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.394 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.538 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.269 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.278 |
MOD_NEK2_2 | 415 | 420 | PF00069 | 0.406 |
MOD_PIKK_1 | 39 | 45 | PF00454 | 0.430 |
MOD_PKA_1 | 270 | 276 | PF00069 | 0.601 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.403 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.598 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.604 |
MOD_PKA_2 | 305 | 311 | PF00069 | 0.595 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.458 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.465 |
MOD_PKA_2 | 440 | 446 | PF00069 | 0.665 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.394 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.359 |
MOD_Plk_4 | 187 | 193 | PF00069 | 0.536 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.335 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.431 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.365 |
MOD_ProDKin_1 | 191 | 197 | PF00069 | 0.431 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.566 |
MOD_SUMO_rev_2 | 54 | 61 | PF00179 | 0.330 |
TRG_DiLeu_BaEn_1 | 408 | 413 | PF01217 | 0.488 |
TRG_DiLeu_BaEn_1 | 80 | 85 | PF01217 | 0.292 |
TRG_DiLeu_BaLyEn_6 | 369 | 374 | PF01217 | 0.516 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.332 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.511 |
TRG_NES_CRM1_1 | 43 | 57 | PF08389 | 0.425 |
TRG_Pf-PMV_PEXEL_1 | 341 | 345 | PF00026 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 372 | 376 | PF00026 | 0.520 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7X3 | Leptomonas seymouri | 72% | 98% |
A0A1X0P4R6 | Trypanosomatidae | 59% | 97% |
A0A3Q8IN33 | Leishmania donovani | 86% | 96% |
A0A3R7MKC3 | Trypanosoma rangeli | 58% | 97% |
A4I153 | Leishmania infantum | 86% | 96% |
D0A5D7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
D0A5D8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 99% |
E9AX87 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 96% |
Q4QA85 | Leishmania major | 86% | 100% |
V5BSX0 | Trypanosoma cruzi | 58% | 97% |