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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 10, no: 0 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
Related structures:
AlphaFold database: A0A3S7WZU9
Term | Name | Level | Count |
---|---|---|---|
GO:0009966 | regulation of signal transduction | 4 | 11 |
GO:0010646 | regulation of cell communication | 4 | 11 |
GO:0023051 | regulation of signaling | 3 | 11 |
GO:0048583 | regulation of response to stimulus | 3 | 11 |
GO:0050789 | regulation of biological process | 2 | 11 |
GO:0050794 | regulation of cellular process | 3 | 11 |
GO:0065007 | biological regulation | 1 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 394 | 398 | PF00656 | 0.399 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 389 | 391 | PF00675 | 0.606 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.618 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.648 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 403 | 405 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 320 | 322 | PF00082 | 0.648 |
CLV_PCSK_PC1ET2_1 | 403 | 405 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.614 |
CLV_PCSK_SKI1_1 | 52 | 56 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.619 |
CLV_Separin_Metazoa | 59 | 63 | PF03568 | 0.379 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.625 |
DEG_SCF_FBW7_1 | 493 | 499 | PF00400 | 0.404 |
DEG_SPOP_SBC_1 | 271 | 275 | PF00917 | 0.403 |
DOC_ANK_TNKS_1 | 38 | 45 | PF00023 | 0.362 |
DOC_CKS1_1 | 493 | 498 | PF01111 | 0.436 |
DOC_CYCLIN_yCln2_LP_2 | 297 | 300 | PF00134 | 0.338 |
DOC_MAPK_gen_1 | 99 | 108 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 22 | 31 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 3 | 11 | PF00069 | 0.486 |
DOC_MAPK_MEF2A_6 | 336 | 344 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 99 | 108 | PF00069 | 0.404 |
DOC_MAPK_RevD_3 | 308 | 321 | PF00069 | 0.362 |
DOC_PP1_RVXF_1 | 31 | 38 | PF00149 | 0.359 |
DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.395 |
DOC_PP2B_LxvP_1 | 92 | 95 | PF13499 | 0.383 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.264 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.340 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.480 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.323 |
DOC_WW_Pin1_4 | 492 | 497 | PF00397 | 0.441 |
LIG_14-3-3_CanoR_1 | 146 | 151 | PF00244 | 0.389 |
LIG_14-3-3_CanoR_1 | 154 | 162 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 240 | 246 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 33 | 38 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 366 | 373 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 390 | 400 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 478 | 487 | PF00244 | 0.363 |
LIG_14-3-3_CterR_2 | 545 | 549 | PF00244 | 0.631 |
LIG_APCC_ABBA_1 | 501 | 506 | PF00400 | 0.352 |
LIG_APCC_ABBA_1 | 544 | 549 | PF00400 | 0.629 |
LIG_BRCT_BRCA1_1 | 119 | 123 | PF00533 | 0.381 |
LIG_BRCT_BRCA1_1 | 514 | 518 | PF00533 | 0.343 |
LIG_EH1_1 | 255 | 263 | PF00400 | 0.332 |
LIG_eIF4E_1 | 256 | 262 | PF01652 | 0.324 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.581 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.398 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.458 |
LIG_FHA_1 | 257 | 263 | PF00498 | 0.348 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.330 |
LIG_FHA_1 | 373 | 379 | PF00498 | 0.370 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.384 |
LIG_FHA_1 | 505 | 511 | PF00498 | 0.355 |
LIG_FHA_1 | 539 | 545 | PF00498 | 0.600 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.286 |
LIG_FHA_2 | 111 | 117 | PF00498 | 0.322 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.414 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.394 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.435 |
LIG_GBD_Chelix_1 | 234 | 242 | PF00786 | 0.533 |
LIG_GBD_Chelix_1 | 290 | 298 | PF00786 | 0.472 |
LIG_LIR_Gen_1 | 211 | 222 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 309 | 319 | PF02991 | 0.325 |
LIG_LIR_Gen_1 | 489 | 498 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 237 | 242 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 286 | 291 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 309 | 314 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 349 | 354 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 382 | 388 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 489 | 493 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 499 | 504 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 68 | 74 | PF02991 | 0.412 |
LIG_MLH1_MIPbox_1 | 119 | 123 | PF16413 | 0.381 |
LIG_NRBOX | 143 | 149 | PF00104 | 0.399 |
LIG_NRBOX | 526 | 532 | PF00104 | 0.443 |
LIG_PCNA_PIPBox_1 | 207 | 216 | PF02747 | 0.374 |
LIG_SH2_PTP2 | 535 | 538 | PF00017 | 0.482 |
LIG_SH2_SRC | 311 | 314 | PF00017 | 0.391 |
LIG_SH2_SRC | 535 | 538 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 256 | 260 | PF00017 | 0.289 |
LIG_SH2_STAP1 | 354 | 358 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 461 | 465 | PF00017 | 0.303 |
LIG_SH2_STAP1 | 504 | 508 | PF00017 | 0.294 |
LIG_SH2_STAP1 | 74 | 78 | PF00017 | 0.370 |
LIG_SH2_STAT3 | 247 | 250 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 516 | 519 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 535 | 538 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.346 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.415 |
LIG_SUMO_SIM_anti_2 | 257 | 262 | PF11976 | 0.250 |
LIG_SUMO_SIM_par_1 | 104 | 114 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 257 | 266 | PF11976 | 0.314 |
LIG_SUMO_SIM_par_1 | 8 | 14 | PF11976 | 0.533 |
LIG_TRAF2_1 | 248 | 251 | PF00917 | 0.452 |
LIG_TRAF2_1 | 489 | 492 | PF00917 | 0.440 |
LIG_TRAF2_1 | 503 | 506 | PF00917 | 0.353 |
LIG_UBA3_1 | 337 | 343 | PF00899 | 0.354 |
LIG_WRC_WIRS_1 | 118 | 123 | PF05994 | 0.359 |
LIG_WW_3 | 298 | 302 | PF00397 | 0.378 |
MOD_CDK_SPxxK_3 | 217 | 224 | PF00069 | 0.402 |
MOD_CDK_SPxxK_3 | 242 | 249 | PF00069 | 0.421 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.380 |
MOD_CK1_1 | 275 | 281 | PF00069 | 0.430 |
MOD_CK1_1 | 346 | 352 | PF00069 | 0.407 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.331 |
MOD_CK1_1 | 483 | 489 | PF00069 | 0.350 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.324 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.395 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.394 |
MOD_CK2_1 | 486 | 492 | PF00069 | 0.353 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.599 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.581 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.526 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.543 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.514 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.613 |
MOD_GlcNHglycan | 420 | 423 | PF01048 | 0.659 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.597 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.616 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.378 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.416 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.412 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.434 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.380 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.360 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.324 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.410 |
MOD_GSK3_1 | 362 | 369 | PF00069 | 0.379 |
MOD_GSK3_1 | 479 | 486 | PF00069 | 0.335 |
MOD_GSK3_1 | 492 | 499 | PF00069 | 0.371 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.375 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.399 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.530 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.551 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.577 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.467 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.398 |
MOD_NEK2_1 | 261 | 266 | PF00069 | 0.309 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.394 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.404 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.354 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.333 |
MOD_NEK2_2 | 496 | 501 | PF00069 | 0.403 |
MOD_PIKK_1 | 275 | 281 | PF00454 | 0.391 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.352 |
MOD_PK_1 | 146 | 152 | PF00069 | 0.409 |
MOD_PK_1 | 249 | 255 | PF00069 | 0.402 |
MOD_PKA_1 | 168 | 174 | PF00069 | 0.392 |
MOD_PKA_1 | 240 | 246 | PF00069 | 0.411 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.465 |
MOD_PKA_2 | 223 | 229 | PF00069 | 0.406 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.411 |
MOD_PKA_2 | 300 | 306 | PF00069 | 0.414 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.327 |
MOD_Plk_1 | 142 | 148 | PF00069 | 0.342 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.358 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.252 |
MOD_Plk_1 | 504 | 510 | PF00069 | 0.401 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.386 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.324 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.348 |
MOD_Plk_4 | 424 | 430 | PF00069 | 0.441 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.342 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.351 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.293 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.437 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.412 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.323 |
MOD_ProDKin_1 | 492 | 498 | PF00069 | 0.438 |
TRG_DiLeu_BaEn_1 | 143 | 148 | PF01217 | 0.395 |
TRG_DiLeu_BaEn_1 | 257 | 262 | PF01217 | 0.250 |
TRG_DiLeu_LyEn_5 | 143 | 148 | PF01217 | 0.395 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 490 | 493 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 535 | 538 | PF00928 | 0.532 |
TRG_ER_diArg_1 | 168 | 170 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 388 | 390 | PF00400 | 0.414 |
TRG_NES_CRM1_1 | 284 | 296 | PF08389 | 0.355 |
TRG_NES_CRM1_1 | 309 | 322 | PF08389 | 0.364 |
TRG_Pf-PMV_PEXEL_1 | 168 | 172 | PF00026 | 0.599 |
TRG_Pf-PMV_PEXEL_1 | 283 | 287 | PF00026 | 0.570 |
TRG_Pf-PMV_PEXEL_1 | 39 | 43 | PF00026 | 0.610 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P650 | Leptomonas seymouri | 61% | 100% |
A0A1X0NSR2 | Trypanosomatidae | 33% | 86% |
A0A3R7MV36 | Trypanosoma rangeli | 34% | 91% |
A4HEW0 | Leishmania braziliensis | 79% | 100% |
A4I233 | Leishmania infantum | 100% | 100% |
C9ZRX2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 92% |
E9AY83 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q990 | Leishmania major | 95% | 100% |
V5BPU6 | Trypanosoma cruzi | 34% | 91% |