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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: A4I853
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 227 | 231 | PF00656 | 0.759 |
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.467 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.741 |
CLV_NRD_NRD_1 | 152 | 154 | PF00675 | 0.768 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.746 |
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 414 | 416 | PF00675 | 0.774 |
CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.661 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.653 |
CLV_PCSK_FUR_1 | 54 | 58 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.737 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.768 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.792 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.663 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.771 |
CLV_PCSK_KEX2_1 | 414 | 416 | PF00082 | 0.774 |
CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 56 | 58 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.653 |
CLV_PCSK_PC1ET2_1 | 247 | 249 | PF00082 | 0.792 |
CLV_PCSK_PC1ET2_1 | 346 | 348 | PF00082 | 0.771 |
CLV_PCSK_PC7_1 | 30 | 36 | PF00082 | 0.662 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.764 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.763 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.761 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.643 |
DEG_SIAH_1 | 119 | 127 | PF03145 | 0.630 |
DOC_CYCLIN_yCln2_LP_2 | 157 | 163 | PF00134 | 0.669 |
DOC_CYCLIN_yCln2_LP_2 | 399 | 405 | PF00134 | 0.756 |
DOC_MAPK_DCC_7 | 396 | 405 | PF00069 | 0.751 |
DOC_MAPK_gen_1 | 171 | 180 | PF00069 | 0.685 |
DOC_MAPK_gen_1 | 244 | 251 | PF00069 | 0.736 |
DOC_MAPK_gen_1 | 396 | 405 | PF00069 | 0.813 |
DOC_PP1_RVXF_1 | 245 | 252 | PF00149 | 0.792 |
DOC_PP2B_LxvP_1 | 399 | 402 | PF13499 | 0.755 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 224 | 228 | PF00917 | 0.629 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 330 | 334 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.742 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.762 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.648 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.816 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.832 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.657 |
LIG_14-3-3_CanoR_1 | 273 | 277 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 332 | 337 | PF00244 | 0.759 |
LIG_14-3-3_CanoR_1 | 423 | 427 | PF00244 | 0.732 |
LIG_BRCT_BRCA1_1 | 321 | 325 | PF00533 | 0.727 |
LIG_CSL_BTD_1 | 221 | 224 | PF09270 | 0.615 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.574 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.820 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.656 |
LIG_FHA_2 | 23 | 29 | PF00498 | 0.658 |
LIG_FHA_2 | 431 | 437 | PF00498 | 0.725 |
LIG_FHA_2 | 63 | 69 | PF00498 | 0.580 |
LIG_LIR_Gen_1 | 254 | 265 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.738 |
LIG_LIR_Nem_3 | 9 | 15 | PF02991 | 0.666 |
LIG_Rb_LxCxE_1 | 38 | 59 | PF01857 | 0.454 |
LIG_SH2_CRK | 12 | 16 | PF00017 | 0.551 |
LIG_SH2_GRB2like | 392 | 395 | PF00017 | 0.699 |
LIG_SH3_1 | 218 | 224 | PF00018 | 0.618 |
LIG_SH3_2 | 114 | 119 | PF14604 | 0.720 |
LIG_SH3_2 | 221 | 226 | PF14604 | 0.615 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.611 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.643 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.794 |
LIG_SH3_3 | 217 | 223 | PF00018 | 0.694 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.701 |
LIG_SUMO_SIM_par_1 | 401 | 407 | PF11976 | 0.758 |
LIG_TRAF2_1 | 7 | 10 | PF00917 | 0.670 |
LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.648 |
LIG_UBA3_1 | 166 | 173 | PF00899 | 0.659 |
MOD_CDC14_SPxK_1 | 360 | 363 | PF00782 | 0.842 |
MOD_CDK_SPK_2 | 239 | 244 | PF00069 | 0.656 |
MOD_CDK_SPK_2 | 404 | 409 | PF00069 | 0.810 |
MOD_CDK_SPxK_1 | 357 | 363 | PF00069 | 0.837 |
MOD_CDK_SPxxK_3 | 239 | 246 | PF00069 | 0.716 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.762 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.823 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.554 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.687 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.718 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.686 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.723 |
MOD_DYRK1A_RPxSP_1 | 127 | 131 | PF00069 | 0.618 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.679 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.726 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.586 |
MOD_GlcNHglycan | 286 | 289 | PF01048 | 0.663 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.711 |
MOD_GlcNHglycan | 321 | 324 | PF01048 | 0.741 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.638 |
MOD_GlcNHglycan | 382 | 385 | PF01048 | 0.707 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.843 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.583 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.682 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.819 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.661 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.612 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.807 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.524 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.649 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.707 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.718 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.513 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.455 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.612 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.657 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.628 |
MOD_N-GLC_1 | 295 | 300 | PF02516 | 0.738 |
MOD_N-GLC_1 | 311 | 316 | PF02516 | 0.609 |
MOD_N-GLC_1 | 415 | 420 | PF02516 | 0.779 |
MOD_N-GLC_2 | 307 | 309 | PF02516 | 0.748 |
MOD_NEK2_2 | 323 | 328 | PF00069 | 0.831 |
MOD_PIKK_1 | 22 | 28 | PF00454 | 0.591 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.794 |
MOD_PIKK_1 | 354 | 360 | PF00454 | 0.715 |
MOD_PIKK_1 | 62 | 68 | PF00454 | 0.590 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.837 |
MOD_PKA_2 | 258 | 264 | PF00069 | 0.785 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.826 |
MOD_PKA_2 | 319 | 325 | PF00069 | 0.688 |
MOD_PKA_2 | 33 | 39 | PF00069 | 0.656 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.781 |
MOD_PKA_2 | 422 | 428 | PF00069 | 0.729 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.628 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.670 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.713 |
MOD_Plk_1 | 295 | 301 | PF00069 | 0.729 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.788 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.812 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.727 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.758 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.762 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.722 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.649 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.816 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.837 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.628 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.656 |
MOD_SUMO_rev_2 | 241 | 249 | PF00179 | 0.792 |
TRG_DiLeu_BaEn_1 | 10 | 15 | PF01217 | 0.662 |
TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.661 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.789 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.764 |
TRG_ER_diArg_1 | 347 | 350 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 396 | 399 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 54 | 57 | PF00400 | 0.478 |
TRG_ER_diArg_1 | 71 | 73 | PF00400 | 0.495 |
TRG_Pf-PMV_PEXEL_1 | 71 | 75 | PF00026 | 0.594 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ITE5 | Leishmania donovani | 99% | 100% |
A4HKM1 | Leishmania braziliensis | 62% | 100% |
E9B310 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q545 | Leishmania major | 85% | 100% |